Canonical Allele Identifier: CA394550963

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778069C>A (hg19) ; chr16:g.3728068C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728068C>A , CM000678.2:g.3728068C>A	GRCh38
NC_000016.9:g.3778069C>A , CM000678.1:g.3778069C>A	GRCh37
NC_000016.8:g.3718070C>A	NCBI36
NG_009873.1:g.157053G>T
NG_009873.2:g.157646G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6979G>T MANE Select	ENSP00000262367.5:p.Ala2327Ser
ENST00000262367.9:c.6979G>T	ENSP00000262367.5:p.Ala2327Ser
ENST00000382070.7:c.6865G>T	ENSP00000371502.3:p.Ala2289Ser
NM_001079846.1:c.6865G>T	NP_001073315.1:p.Ala2289Ser
NM_004380.2:c.6979G>T	NP_004371.2:p.Ala2327Ser
XM_005255124.3:c.6934G>T	XP_005255181.1:p.Ala2312Ser
XM_005255125.3:c.6562G>T	XP_005255182.1:p.Ala2188Ser
XM_006720848.2:c.6718G>T	XP_006720911.1:p.Ala2240Ser
XM_011522380.1:c.6925G>T	XP_011520682.1:p.Ala2309Ser
XM_011522381.1:c.6226G>T	XP_011520683.1:p.Ala2076Ser
XM_005255124.4:c.6934G>T	XP_005255181.1:p.Ala2312Ser
XM_005255125.4:c.6562G>T	XP_005255182.1:p.Ala2188Ser
XM_006720848.3:c.6718G>T	XP_006720911.1:p.Ala2240Ser
XM_011522381.2:c.6226G>T	XP_011520683.1:p.Ala2076Ser
XM_017022944.1:c.6973G>T	XP_016878433.1:p.Ala2325Ser
NM_004380.3:c.6979G>T MANE Select	NP_004371.2:p.Ala2327Ser