Canonical Allele Identifier: CA1041681072

Gene: CREB1

Linked Data

• dbSNP Id: rs10932201
• gnomAD v3: 2-207561533-G-C
• gnomAD v4: 2-207561533-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.207561533G>C , CM000664.2:g.207561533G>C	GRCh38
NC_000002.11:g.208426257G>C , CM000664.1:g.208426257G>C	GRCh37
NC_000002.10:g.208134502G>C	NCBI36
NG_023299.1:g.36642G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000353267.8:c.261+1161G>C MANE Select	ENSP00000236995.3:n.261+1161G>C
ENST00000353267.7:c.261+1161G>C	ENSP00000236995.3:n.261+1161G>C
ENST00000418081.5:c.101+373G>C
ENST00000421139.5:c.141+1161G>C	ENSP00000403678.1:n.141+1161G>C
ENST00000430624.5:c.261+1161G>C	ENSP00000405539.1:n.261+1161G>C
ENST00000432329.6:c.303+373G>C	ENSP00000387699.2:n.303+373G>C
ENST00000445803.5:c.303+373G>C	ENSP00000407227.1:n.303+373G>C
ENST00000448277.5:c.141+1161G>C	ENSP00000405711.1:n.141+1161G>C
ENST00000452474.5:c.303+373G>C	ENSP00000392428.1:n.303+373G>C
ENST00000457101.5:c.183+373G>C	ENSP00000391125.1:n.183+373G>C
ENST00000464407.1:n.232+1161G>C
ENST00000480189.5:n.281+1161G>C
ENST00000494094.5:n.332+1161G>C
NM_004379.3:c.261+1161G>C	NP_004370.1:n.261+1161G>C
NM_134442.3:c.303+373G>C	NP_604391.1:n.303+373G>C
XM_011510645.1:c.303+373G>C	XP_011508947.1:n.303+373G>C
XM_011510646.1:c.303+373G>C	XP_011508948.1:n.303+373G>C
XM_011510647.1:c.261+1161G>C	XP_011508949.1:n.261+1161G>C
XM_011510648.1:c.303+373G>C	XP_011508950.1:n.303+373G>C
XM_011510649.1:c.183+373G>C	XP_011508951.1:n.183+373G>C
XM_011510650.1:c.183+373G>C	XP_011508952.1:n.183+373G>C
XM_011510651.1:c.141+1161G>C	XP_011508953.1:n.141+1161G>C
XM_011510652.1:c.303+373G>C	XP_011508954.1:n.303+373G>C
XM_011510653.1:c.-321+1161G>C	XP_011508955.1:n.-321+1161G>C
XR_241289.1:n.530+373G>C
XR_241290.1:n.530+373G>C
XR_241292.1:n.530+373G>C
XR_427071.1:n.462+1161G>C
XR_922862.1:n.318+373G>C
NM_001320793.1:c.261+1161G>C	NP_001307722.1:n.261+1161G>C
NM_004379.4:c.261+1161G>C	NP_004370.1:n.261+1161G>C
NM_134442.4:c.303+373G>C	NP_604391.1:n.303+373G>C
NR_135473.1:n.554+373G>C
XM_011510646.3:c.303+373G>C	XP_011508948.1:n.303+373G>C
XM_011510647.3:c.261+1161G>C	XP_011508949.1:n.261+1161G>C
XM_011510648.3:c.303+373G>C	XP_011508950.1:n.303+373G>C
XM_011510650.3:c.183+373G>C	XP_011508952.1:n.183+373G>C
XM_011510651.2:c.141+1161G>C	XP_011508953.1:n.141+1161G>C
XM_017003399.2:c.261+1161G>C	XP_016858888.1:n.261+1161G>C
XM_017003401.2:c.-451+373G>C	XP_016858890.1:n.-451+373G>C
XR_001738634.2:n.442+1161G>C
XR_001738635.2:n.374+1161G>C
XR_001738636.2:n.503+373G>C
XR_001738637.2:n.442+1161G>C
XR_241290.2:n.503+373G>C
XR_241292.2:n.503+373G>C
NM_004379.5:c.261+1161G>C MANE Select	NP_004370.1:n.261+1161G>C
NM_001320793.2:c.261+1161G>C	NP_001307722.1:n.261+1161G>C
NM_001371426.1:c.303+373G>C	NP_001358355.1:n.303+373G>C
NM_001371427.1:c.261+1161G>C	NP_001358356.1:n.261+1161G>C
NM_001371428.1:c.141+1161G>C	NP_001358357.1:n.141+1161G>C
NM_134442.5:c.303+373G>C	NP_604391.1:n.303+373G>C
NR_135473.2:n.484+373G>C
NR_163946.1:n.442+1161G>C
NR_163947.1:n.326+1161G>C