Canonical Allele Identifier: CA394563985

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151329977
• MyVariant Identifiers: chr16:g.3786785G>A (hg19) ; chr16:g.3736784G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736784G>A , CM000678.2:g.3736784G>A	GRCh38
NC_000016.9:g.3786785G>A , CM000678.1:g.3786785G>A	GRCh37
NC_000016.8:g.3726786G>A	NCBI36
NG_009873.1:g.148337C>T
NG_009873.2:g.148930C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4426C>T MANE Select	ENSP00000262367.5:p.Pro1476Ser
ENST00000262367.9:c.4426C>T	ENSP00000262367.5:p.Pro1476Ser
ENST00000382070.7:c.4312C>T	ENSP00000371502.3:p.Pro1438Ser
ENST00000570939.2:c.3061C>T	ENSP00000461002.2:p.Pro1021Ser
ENST00000571763.5:n.216C>T
ENST00000574740.1:n.247C>T
ENST00000576720.1:n.3249C>T
NM_001079846.1:c.4312C>T	NP_001073315.1:p.Pro1438Ser
NM_004380.2:c.4426C>T	NP_004371.2:p.Pro1476Ser
XM_005255124.3:c.4381C>T	XP_005255181.1:p.Pro1461Ser
XM_005255125.3:c.4009C>T	XP_005255182.1:p.Pro1337Ser
XM_006720848.2:c.4165C>T	XP_006720911.1:p.Pro1389Ser
XM_011522380.1:c.4372C>T	XP_011520682.1:p.Pro1458Ser
XM_011522381.1:c.3673C>T	XP_011520683.1:p.Pro1225Ser
XM_005255124.4:c.4381C>T	XP_005255181.1:p.Pro1461Ser
XM_005255125.4:c.4009C>T	XP_005255182.1:p.Pro1337Ser
XM_006720848.3:c.4165C>T	XP_006720911.1:p.Pro1389Ser
XM_011522381.2:c.3673C>T	XP_011520683.1:p.Pro1225Ser
XM_017022944.1:c.4420C>T	XP_016878433.1:p.Pro1474Ser
NM_004380.3:c.4426C>T MANE Select	NP_004371.2:p.Pro1476Ser