Canonical Allele Identifier: CA394554793

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779080T>A (hg19) ; chr16:g.3729079T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729079T>A , CM000678.2:g.3729079T>A	GRCh38
NC_000016.9:g.3779080T>A , CM000678.1:g.3779080T>A	GRCh37
NC_000016.8:g.3719081T>A	NCBI36
NG_009873.1:g.156042A>T
NG_009873.2:g.156635A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5968A>T MANE Select	ENSP00000262367.5:p.Thr1990Ser
ENST00000262367.9:c.5968A>T	ENSP00000262367.5:p.Thr1990Ser
ENST00000382070.7:c.5854A>T	ENSP00000371502.3:p.Thr1952Ser
NM_001079846.1:c.5854A>T	NP_001073315.1:p.Thr1952Ser
NM_004380.2:c.5968A>T	NP_004371.2:p.Thr1990Ser
XM_005255124.3:c.5923A>T	XP_005255181.1:p.Thr1975Ser
XM_005255125.3:c.5551A>T	XP_005255182.1:p.Thr1851Ser
XM_006720848.2:c.5707A>T	XP_006720911.1:p.Thr1903Ser
XM_011522380.1:c.5914A>T	XP_011520682.1:p.Thr1972Ser
XM_011522381.1:c.5215A>T	XP_011520683.1:p.Thr1739Ser
XM_005255124.4:c.5923A>T	XP_005255181.1:p.Thr1975Ser
XM_005255125.4:c.5551A>T	XP_005255182.1:p.Thr1851Ser
XM_006720848.3:c.5707A>T	XP_006720911.1:p.Thr1903Ser
XM_011522381.2:c.5215A>T	XP_011520683.1:p.Thr1739Ser
XM_017022944.1:c.5962A>T	XP_016878433.1:p.Thr1988Ser
NM_004380.3:c.5968A>T MANE Select	NP_004371.2:p.Thr1990Ser