Canonical Allele Identifier: CA394550310

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151298598
• MyVariant Identifiers: chr16:g.3777842G>C (hg19) ; chr16:g.3727841G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727841G>C , CM000678.2:g.3727841G>C	GRCh38
NC_000016.9:g.3777842G>C , CM000678.1:g.3777842G>C	GRCh37
NC_000016.8:g.3717843G>C	NCBI36
NG_009873.1:g.157280C>G
NG_009873.2:g.157873C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7206C>G MANE Select	ENSP00000262367.5:p.Asn2402Lys
ENST00000262367.9:c.7206C>G	ENSP00000262367.5:p.Asn2402Lys
ENST00000382070.7:c.7092C>G	ENSP00000371502.3:p.Asn2364Lys
NM_001079846.1:c.7092C>G	NP_001073315.1:p.Asn2364Lys
NM_004380.2:c.7206C>G	NP_004371.2:p.Asn2402Lys
XM_005255124.3:c.7161C>G	XP_005255181.1:p.Asn2387Lys
XM_005255125.3:c.6789C>G	XP_005255182.1:p.Asn2263Lys
XM_006720848.2:c.6945C>G	XP_006720911.1:p.Asn2315Lys
XM_011522380.1:c.7152C>G	XP_011520682.1:p.Asn2384Lys
XM_011522381.1:c.6453C>G	XP_011520683.1:p.Asn2151Lys
XM_005255124.4:c.7161C>G	XP_005255181.1:p.Asn2387Lys
XM_005255125.4:c.6789C>G	XP_005255182.1:p.Asn2263Lys
XM_006720848.3:c.6945C>G	XP_006720911.1:p.Asn2315Lys
XM_011522381.2:c.6453C>G	XP_011520683.1:p.Asn2151Lys
XM_017022944.1:c.7200C>G	XP_016878433.1:p.Asn2400Lys
NM_004380.3:c.7206C>G MANE Select	NP_004371.2:p.Asn2402Lys