Canonical Allele Identifier: CA394554197

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778936G>T (hg19) ; chr16:g.3728935G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728935G>T , CM000678.2:g.3728935G>T	GRCh38
NC_000016.9:g.3778936G>T , CM000678.1:g.3778936G>T	GRCh37
NC_000016.8:g.3718937G>T	NCBI36
NG_009873.1:g.156186C>A
NG_009873.2:g.156779C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.6112C>A MANE Select	ENSP00000262367.5:p.Pro2038Thr
ENST00000262367.9:c.6112C>A	ENSP00000262367.5:p.Pro2038Thr
ENST00000382070.7:c.5998C>A	ENSP00000371502.3:p.Pro2000Thr
NM_001079846.1:c.5998C>A	NP_001073315.1:p.Pro2000Thr
NM_004380.2:c.6112C>A	NP_004371.2:p.Pro2038Thr
XM_005255124.3:c.6067C>A	XP_005255181.1:p.Pro2023Thr
XM_005255125.3:c.5695C>A	XP_005255182.1:p.Pro1899Thr
XM_006720848.2:c.5851C>A	XP_006720911.1:p.Pro1951Thr
XM_011522380.1:c.6058C>A	XP_011520682.1:p.Pro2020Thr
XM_011522381.1:c.5359C>A	XP_011520683.1:p.Pro1787Thr
XM_005255124.4:c.6067C>A	XP_005255181.1:p.Pro2023Thr
XM_005255125.4:c.5695C>A	XP_005255182.1:p.Pro1899Thr
XM_006720848.3:c.5851C>A	XP_006720911.1:p.Pro1951Thr
XM_011522381.2:c.5359C>A	XP_011520683.1:p.Pro1787Thr
XM_017022944.1:c.6106C>A	XP_016878433.1:p.Pro2036Thr
NM_004380.3:c.6112C>A MANE Select	NP_004371.2:p.Pro2038Thr