Canonical Allele Identifier: CA394554034
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728889A>C , CM000678.2:g.3728889A>C GRCh38
NC_000016.9:g.3778890A>C , CM000678.1:g.3778890A>C GRCh37
NC_000016.8:g.3718891A>C NCBI36
NG_009873.1:g.156232T>G
NG_009873.2:g.156825T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6158T>G MANE Select ENSP00000262367.5:p.Met2053Arg
ENST00000262367.9:c.6158T>G ENSP00000262367.5:p.Met2053Arg
ENST00000382070.7:c.6044T>G ENSP00000371502.3:p.Met2015Arg
NM_001079846.1:c.6044T>G NP_001073315.1:p.Met2015Arg
NM_004380.2:c.6158T>G NP_004371.2:p.Met2053Arg
XM_005255124.3:c.6113T>G XP_005255181.1:p.Met2038Arg
XM_005255125.3:c.5741T>G XP_005255182.1:p.Met1914Arg
XM_006720848.2:c.5897T>G XP_006720911.1:p.Met1966Arg
XM_011522380.1:c.6104T>G XP_011520682.1:p.Met2035Arg
XM_011522381.1:c.5405T>G XP_011520683.1:p.Met1802Arg
XM_005255124.4:c.6113T>G XP_005255181.1:p.Met2038Arg
XM_005255125.4:c.5741T>G XP_005255182.1:p.Met1914Arg
XM_006720848.3:c.5897T>G XP_006720911.1:p.Met1966Arg
XM_011522381.2:c.5405T>G XP_011520683.1:p.Met1802Arg
XM_017022944.1:c.6152T>G XP_016878433.1:p.Met2051Arg
NM_004380.3:c.6158T>G MANE Select NP_004371.2:p.Met2053Arg