Canonical Allele Identifier: CA64879582
Gene: CREB1 HGNC NCBI

Linked Data

dbSNP Id: rs2254137

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.207579304C>A , CM000664.2:g.207579304C>A GRCh38
NC_000002.11:g.208444028C>A , CM000664.1:g.208444028C>A GRCh37
NC_000002.10:g.208152273C>A NCBI36
NG_023299.1:g.54413C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000353267.8:c.839+1649C>A MANE Select ENSP00000236995.3:n.839+1649C>A
ENST00000353267.7:c.839+1649C>A ENSP00000236995.3:n.839+1649C>A
ENST00000418081.5:c.857+1649C>A
ENST00000430624.5:c.839+1649C>A ENSP00000405539.1:n.839+1649C>A
ENST00000432329.6:c.881+1649C>A ENSP00000387699.2:n.881+1649C>A
ENST00000448277.5:c.719+1649C>A ENSP00000405711.1:n.719+1649C>A
ENST00000494983.1:n.209+1649C>A
NM_004379.3:c.839+1649C>A NP_004370.1:n.839+1649C>A
NM_134442.3:c.881+1649C>A NP_604391.1:n.881+1649C>A
XM_011510645.1:c.881+1649C>A XP_011508947.1:n.881+1649C>A
XM_011510646.1:c.881+1649C>A XP_011508948.1:n.881+1649C>A
XM_011510647.1:c.839+1649C>A XP_011508949.1:n.839+1649C>A
XM_011510648.1:c.882-217C>A XP_011508950.1:n.882-217C>A
XM_011510649.1:c.761+1649C>A XP_011508951.1:n.761+1649C>A
XM_011510650.1:c.761+1649C>A XP_011508952.1:n.761+1649C>A
XM_011510651.1:c.719+1649C>A XP_011508953.1:n.719+1649C>A
XM_011510653.1:c.383+1649C>A XP_011508955.1:n.383+1649C>A
XR_241289.1:n.1108+1649C>A
XR_241290.1:n.1286+1649C>A
XR_241292.1:n.1171+1649C>A
XR_427071.1:n.1103+1649C>A
XR_922862.1:n.1199+1649C>A
NM_004379.4:c.839+1649C>A NP_004370.1:n.839+1649C>A
NM_134442.4:c.881+1649C>A NP_604391.1:n.881+1649C>A
NR_135473.1:n.1132+1649C>A
XM_011510646.3:c.881+1649C>A XP_011508948.1:n.881+1649C>A
XM_011510647.3:c.839+1649C>A XP_011508949.1:n.839+1649C>A
XM_011510648.3:c.882-217C>A XP_011508950.1:n.882-217C>A
XM_011510650.3:c.761+1649C>A XP_011508952.1:n.761+1649C>A
XM_011510651.2:c.719+1649C>A XP_011508953.1:n.719+1649C>A
XM_017003399.2:c.840-217C>A XP_016858888.1:n.840-217C>A
XM_017003401.2:c.191+1649C>A XP_016858890.1:n.191+1649C>A
XR_001738634.2:n.1020+1649C>A
XR_001738635.2:n.952+1649C>A
XR_001738636.2:n.1675+1649C>A
XR_001738637.2:n.1614+1649C>A
XR_241290.2:n.1259+1649C>A
XR_241292.2:n.1144+1649C>A
NM_004379.5:c.839+1649C>A MANE Select NP_004370.1:n.839+1649C>A
NM_001371426.1:c.881+1649C>A NP_001358355.1:n.881+1649C>A
NM_001371427.1:c.839+1649C>A NP_001358356.1:n.839+1649C>A
NM_001371428.1:c.719+1649C>A NP_001358357.1:n.719+1649C>A
NM_134442.5:c.881+1649C>A NP_604391.1:n.881+1649C>A
NR_135473.2:n.1062+1649C>A
NR_163946.1:n.1020+1649C>A
NR_163947.1:n.904+1649C>A