Canonical Allele Identifier: CA394568747

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3807899C>A (hg19) ; chr16:g.3757898C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3757898C>A , CM000678.2:g.3757898C>A	GRCh38
NC_000016.9:g.3807899C>A , CM000678.1:g.3807899C>A	GRCh37
NC_000016.8:g.3747900C>A	NCBI36
NG_009873.1:g.127223G>T
NG_009873.2:g.127816G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.3520G>T MANE Select	ENSP00000262367.5:p.Val1174Phe
ENST00000262367.9:c.3520G>T	ENSP00000262367.5:p.Val1174Phe
ENST00000382070.7:c.3406G>T	ENSP00000371502.3:p.Val1136Phe
ENST00000570939.2:c.2125G>T	ENSP00000461002.2:p.Val709Phe
NM_001079846.1:c.3406G>T	NP_001073315.1:p.Val1136Phe
NM_004380.2:c.3520G>T	NP_004371.2:p.Val1174Phe
XM_005255124.3:c.3475G>T	XP_005255181.1:p.Val1159Phe
XM_005255125.3:c.3103G>T	XP_005255182.1:p.Val1035Phe
XM_006720848.2:c.3520G>T	XP_006720911.1:p.Val1174Phe
XM_011522380.1:c.3466G>T	XP_011520682.1:p.Val1156Phe
XM_011522381.1:c.2767G>T	XP_011520683.1:p.Val923Phe
XM_011522382.1:c.3520G>T	XP_011520684.1:p.Val1174Phe
XM_005255124.4:c.3475G>T	XP_005255181.1:p.Val1159Phe
XM_005255125.4:c.3103G>T	XP_005255182.1:p.Val1035Phe
XM_006720848.3:c.3520G>T	XP_006720911.1:p.Val1174Phe
XM_011522381.2:c.2767G>T	XP_011520683.1:p.Val923Phe
XM_011522382.3:c.3520G>T	XP_011520684.1:p.Val1174Phe
XM_017022944.1:c.3514G>T	XP_016878433.1:p.Val1172Phe
NM_004380.3:c.3520G>T MANE Select	NP_004371.2:p.Val1174Phe