Canonical Allele Identifier: CA394556420

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310850
• MyVariant Identifiers: chr16:g.3779615C>A (hg19) ; chr16:g.3729614C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729614C>A , CM000678.2:g.3729614C>A	GRCh38
NC_000016.9:g.3779615C>A , CM000678.1:g.3779615C>A	GRCh37
NC_000016.8:g.3719616C>A	NCBI36
NG_009873.1:g.155507G>T
NG_009873.2:g.156100G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5433G>T MANE Select	ENSP00000262367.5:p.Lys1811Asn
ENST00000262367.9:c.5433G>T	ENSP00000262367.5:p.Lys1811Asn
ENST00000382070.7:c.5319G>T	ENSP00000371502.3:p.Lys1773Asn
NM_001079846.1:c.5319G>T	NP_001073315.1:p.Lys1773Asn
NM_004380.2:c.5433G>T	NP_004371.2:p.Lys1811Asn
XM_005255124.3:c.5388G>T	XP_005255181.1:p.Lys1796Asn
XM_005255125.3:c.5016G>T	XP_005255182.1:p.Lys1672Asn
XM_006720848.2:c.5172G>T	XP_006720911.1:p.Lys1724Asn
XM_011522380.1:c.5379G>T	XP_011520682.1:p.Lys1793Asn
XM_011522381.1:c.4680G>T	XP_011520683.1:p.Lys1560Asn
XM_005255124.4:c.5388G>T	XP_005255181.1:p.Lys1796Asn
XM_005255125.4:c.5016G>T	XP_005255182.1:p.Lys1672Asn
XM_006720848.3:c.5172G>T	XP_006720911.1:p.Lys1724Asn
XM_011522381.2:c.4680G>T	XP_011520683.1:p.Lys1560Asn
XM_017022944.1:c.5427G>T	XP_016878433.1:p.Lys1809Asn
NM_004380.3:c.5433G>T MANE Select	NP_004371.2:p.Lys1811Asn