Canonical Allele Identifier: CA64877704

Gene: CREB1

Linked Data

• dbSNP Id: rs35261053
• MyVariant Identifiers: chr2:g.208426276_208426277insC (hg19) ; chr2:g.207561552_207561553insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.207561552_207561553insC , CM000664.2:g.207561552_207561553insC	GRCh38
NC_000002.11:g.208426276_208426277insC , CM000664.1:g.208426276_208426277insC	GRCh37
NC_000002.10:g.208134521_208134522insC	NCBI36
NG_023299.1:g.36661_36662insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353267.8:c.261+1180_261+1181insC MANE Select	ENSP00000236995.3:n.261+1180_261+1181insC
ENST00000353267.7:c.261+1180_261+1181insC	ENSP00000236995.3:n.261+1180_261+1181insC
ENST00000418081.5:c.101+392_101+393insC
ENST00000421139.5:c.141+1180_141+1181insC	ENSP00000403678.1:n.141+1180_141+1181insC
ENST00000430624.5:c.261+1180_261+1181insC	ENSP00000405539.1:n.261+1180_261+1181insC
ENST00000432329.6:c.303+392_303+393insC	ENSP00000387699.2:n.303+392_303+393insC
ENST00000445803.5:c.303+392_303+393insC	ENSP00000407227.1:n.303+392_303+393insC
ENST00000448277.5:c.141+1180_141+1181insC	ENSP00000405711.1:n.141+1180_141+1181insC
ENST00000452474.5:c.303+392_303+393insC	ENSP00000392428.1:n.303+392_303+393insC
ENST00000457101.5:c.183+392_183+393insC	ENSP00000391125.1:n.183+392_183+393insC
ENST00000464407.1:n.232+1180_232+1181insC
ENST00000480189.5:n.281+1180_281+1181insC
ENST00000494094.5:n.332+1180_332+1181insC
NM_004379.3:c.261+1180_261+1181insC	NP_004370.1:n.261+1180_261+1181insC
NM_134442.3:c.303+392_303+393insC	NP_604391.1:n.303+392_303+393insC
XM_011510645.1:c.303+392_303+393insC	XP_011508947.1:n.303+392_303+393insC
XM_011510646.1:c.303+392_303+393insC	XP_011508948.1:n.303+392_303+393insC
XM_011510647.1:c.261+1180_261+1181insC	XP_011508949.1:n.261+1180_261+1181insC
XM_011510648.1:c.303+392_303+393insC	XP_011508950.1:n.303+392_303+393insC
XM_011510649.1:c.183+392_183+393insC	XP_011508951.1:n.183+392_183+393insC
XM_011510650.1:c.183+392_183+393insC	XP_011508952.1:n.183+392_183+393insC
XM_011510651.1:c.141+1180_141+1181insC	XP_011508953.1:n.141+1180_141+1181insC
XM_011510652.1:c.303+392_303+393insC	XP_011508954.1:n.303+392_303+393insC
XM_011510653.1:c.-321+1180_-321+1181insC	XP_011508955.1:n.-321+1180_-321+1181insC
XR_241289.1:n.530+392_530+393insC
XR_241290.1:n.530+392_530+393insC
XR_241292.1:n.530+392_530+393insC
XR_427071.1:n.462+1180_462+1181insC
XR_922862.1:n.318+392_318+393insC
NM_001320793.1:c.261+1180_261+1181insC	NP_001307722.1:n.261+1180_261+1181insC
NM_004379.4:c.261+1180_261+1181insC	NP_004370.1:n.261+1180_261+1181insC
NM_134442.4:c.303+392_303+393insC	NP_604391.1:n.303+392_303+393insC
NR_135473.1:n.554+392_554+393insC
XM_011510646.3:c.303+392_303+393insC	XP_011508948.1:n.303+392_303+393insC
XM_011510647.3:c.261+1180_261+1181insC	XP_011508949.1:n.261+1180_261+1181insC
XM_011510648.3:c.303+392_303+393insC	XP_011508950.1:n.303+392_303+393insC
XM_011510650.3:c.183+392_183+393insC	XP_011508952.1:n.183+392_183+393insC
XM_011510651.2:c.141+1180_141+1181insC	XP_011508953.1:n.141+1180_141+1181insC
XM_017003399.2:c.261+1180_261+1181insC	XP_016858888.1:n.261+1180_261+1181insC
XM_017003401.2:c.-451+392_-451+393insC	XP_016858890.1:n.-451+392_-451+393insC
XR_001738634.2:n.442+1180_442+1181insC
XR_001738635.2:n.374+1180_374+1181insC
XR_001738636.2:n.503+392_503+393insC
XR_001738637.2:n.442+1180_442+1181insC
XR_241290.2:n.503+392_503+393insC
XR_241292.2:n.503+392_503+393insC
NM_004379.5:c.261+1180_261+1181insC MANE Select	NP_004370.1:n.261+1180_261+1181insC
NM_001320793.2:c.261+1180_261+1181insC	NP_001307722.1:n.261+1180_261+1181insC
NM_001371426.1:c.303+392_303+393insC	NP_001358355.1:n.303+392_303+393insC
NM_001371427.1:c.261+1180_261+1181insC	NP_001358356.1:n.261+1180_261+1181insC
NM_001371428.1:c.141+1180_141+1181insC	NP_001358357.1:n.141+1180_141+1181insC
NM_134442.5:c.303+392_303+393insC	NP_604391.1:n.303+392_303+393insC
NR_135473.2:n.484+392_484+393insC
NR_163946.1:n.442+1180_442+1181insC
NR_163947.1:n.326+1180_326+1181insC