Canonical Allele Identifier: CA1323674930

Gene: CREB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.207561549_207561554delinsCTAGAT , CM000664.2:g.207561549_207561554delinsCTAGAT	GRCh38
NC_000002.11:g.208426273_208426278delinsCTAGAT , CM000664.1:g.208426273_208426278delinsCTAGAT	GRCh37
NC_000002.10:g.208134518_208134523delinsCTAGAT	NCBI36
NG_023299.1:g.36658_36663delinsCTAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353267.8:c.261+1177_261+1182delinsCTAGAT MANE Select	ENSP00000236995.3:n.261+1177_261+1182delinsCTAGAT
ENST00000353267.7:c.261+1177_261+1182delinsCTAGAT	ENSP00000236995.3:n.261+1177_261+1182delinsCTAGAT
ENST00000418081.5:c.101+389_101+394delinsCTAGAT
ENST00000421139.5:c.141+1177_141+1182delinsCTAGAT	ENSP00000403678.1:n.141+1177_141+1182delinsCTAGAT
ENST00000430624.5:c.261+1177_261+1182delinsCTAGAT	ENSP00000405539.1:n.261+1177_261+1182delinsCTAGAT
ENST00000432329.6:c.303+389_303+394delinsCTAGAT	ENSP00000387699.2:n.303+389_303+394delinsCTAGAT
ENST00000445803.5:c.303+389_303+394delinsCTAGAT	ENSP00000407227.1:n.303+389_303+394delinsCTAGAT
ENST00000448277.5:c.141+1177_141+1182delinsCTAGAT	ENSP00000405711.1:n.141+1177_141+1182delinsCTAGAT
ENST00000452474.5:c.303+389_303+394delinsCTAGAT	ENSP00000392428.1:n.303+389_303+394delinsCTAGAT
ENST00000457101.5:c.183+389_183+394delinsCTAGAT	ENSP00000391125.1:n.183+389_183+394delinsCTAGAT
ENST00000464407.1:n.232+1177_232+1182delinsCTAGAT
ENST00000480189.5:n.281+1177_281+1182delinsCTAGAT
ENST00000494094.5:n.332+1177_332+1182delinsCTAGAT
NM_004379.3:c.261+1177_261+1182delinsCTAGAT	NP_004370.1:n.261+1177_261+1182delinsCTAGAT
NM_134442.3:c.303+389_303+394delinsCTAGAT	NP_604391.1:n.303+389_303+394delinsCTAGAT
XM_011510645.1:c.303+389_303+394delinsCTAGAT	XP_011508947.1:n.303+389_303+394delinsCTAGAT
XM_011510646.1:c.303+389_303+394delinsCTAGAT	XP_011508948.1:n.303+389_303+394delinsCTAGAT
XM_011510647.1:c.261+1177_261+1182delinsCTAGAT	XP_011508949.1:n.261+1177_261+1182delinsCTAGAT
XM_011510648.1:c.303+389_303+394delinsCTAGAT	XP_011508950.1:n.303+389_303+394delinsCTAGAT
XM_011510649.1:c.183+389_183+394delinsCTAGAT	XP_011508951.1:n.183+389_183+394delinsCTAGAT
XM_011510650.1:c.183+389_183+394delinsCTAGAT	XP_011508952.1:n.183+389_183+394delinsCTAGAT
XM_011510651.1:c.141+1177_141+1182delinsCTAGAT	XP_011508953.1:n.141+1177_141+1182delinsCTAGAT
XM_011510652.1:c.303+389_303+394delinsCTAGAT	XP_011508954.1:n.303+389_303+394delinsCTAGAT
XM_011510653.1:c.-321+1177_-321+1182delinsCTAGAT	XP_011508955.1:n.-321+1177_-321+1182delinsCTAGAT
XR_241289.1:n.530+389_530+394delinsCTAGAT
XR_241290.1:n.530+389_530+394delinsCTAGAT
XR_241292.1:n.530+389_530+394delinsCTAGAT
XR_427071.1:n.462+1177_462+1182delinsCTAGAT
XR_922862.1:n.318+389_318+394delinsCTAGAT
NM_001320793.1:c.261+1177_261+1182delinsCTAGAT	NP_001307722.1:n.261+1177_261+1182delinsCTAGAT
NM_004379.4:c.261+1177_261+1182delinsCTAGAT	NP_004370.1:n.261+1177_261+1182delinsCTAGAT
NM_134442.4:c.303+389_303+394delinsCTAGAT	NP_604391.1:n.303+389_303+394delinsCTAGAT
NR_135473.1:n.554+389_554+394delinsCTAGAT
XM_011510646.3:c.303+389_303+394delinsCTAGAT	XP_011508948.1:n.303+389_303+394delinsCTAGAT
XM_011510647.3:c.261+1177_261+1182delinsCTAGAT	XP_011508949.1:n.261+1177_261+1182delinsCTAGAT
XM_011510648.3:c.303+389_303+394delinsCTAGAT	XP_011508950.1:n.303+389_303+394delinsCTAGAT
XM_011510650.3:c.183+389_183+394delinsCTAGAT	XP_011508952.1:n.183+389_183+394delinsCTAGAT
XM_011510651.2:c.141+1177_141+1182delinsCTAGAT	XP_011508953.1:n.141+1177_141+1182delinsCTAGAT
XM_017003399.2:c.261+1177_261+1182delinsCTAGAT	XP_016858888.1:n.261+1177_261+1182delinsCTAGAT
XM_017003401.2:c.-451+389_-451+394delinsCTAGAT	XP_016858890.1:n.-451+389_-451+394delinsCTAGAT
XR_001738634.2:n.442+1177_442+1182delinsCTAGAT
XR_001738635.2:n.374+1177_374+1182delinsCTAGAT
XR_001738636.2:n.503+389_503+394delinsCTAGAT
XR_001738637.2:n.442+1177_442+1182delinsCTAGAT
XR_241290.2:n.503+389_503+394delinsCTAGAT
XR_241292.2:n.503+389_503+394delinsCTAGAT
NM_004379.5:c.261+1177_261+1182delinsCTAGAT MANE Select	NP_004370.1:n.261+1177_261+1182delinsCTAGAT
NM_001320793.2:c.261+1177_261+1182delinsCTAGAT	NP_001307722.1:n.261+1177_261+1182delinsCTAGAT
NM_001371426.1:c.303+389_303+394delinsCTAGAT	NP_001358355.1:n.303+389_303+394delinsCTAGAT
NM_001371427.1:c.261+1177_261+1182delinsCTAGAT	NP_001358356.1:n.261+1177_261+1182delinsCTAGAT
NM_001371428.1:c.141+1177_141+1182delinsCTAGAT	NP_001358357.1:n.141+1177_141+1182delinsCTAGAT
NM_134442.5:c.303+389_303+394delinsCTAGAT	NP_604391.1:n.303+389_303+394delinsCTAGAT
NR_135473.2:n.484+389_484+394delinsCTAGAT
NR_163946.1:n.442+1177_442+1182delinsCTAGAT
NR_163947.1:n.326+1177_326+1182delinsCTAGAT