Canonical Allele Identifier: CA394551142
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs768181832

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728106A>T , CM000678.2:g.3728106A>T GRCh38
NC_000016.9:g.3778107A>T , CM000678.1:g.3778107A>T GRCh37
NC_000016.8:g.3718108A>T NCBI36
NG_009873.1:g.157015T>A
NG_009873.2:g.157608T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6941T>A MANE Select ENSP00000262367.5:p.Met2314Lys
ENST00000262367.9:c.6941T>A ENSP00000262367.5:p.Met2314Lys
ENST00000382070.7:c.6827T>A ENSP00000371502.3:p.Met2276Lys
NM_001079846.1:c.6827T>A NP_001073315.1:p.Met2276Lys
NM_004380.2:c.6941T>A NP_004371.2:p.Met2314Lys
XM_005255124.3:c.6896T>A XP_005255181.1:p.Met2299Lys
XM_005255125.3:c.6524T>A XP_005255182.1:p.Met2175Lys
XM_006720848.2:c.6680T>A XP_006720911.1:p.Met2227Lys
XM_011522380.1:c.6887T>A XP_011520682.1:p.Met2296Lys
XM_011522381.1:c.6188T>A XP_011520683.1:p.Met2063Lys
XM_005255124.4:c.6896T>A XP_005255181.1:p.Met2299Lys
XM_005255125.4:c.6524T>A XP_005255182.1:p.Met2175Lys
XM_006720848.3:c.6680T>A XP_006720911.1:p.Met2227Lys
XM_011522381.2:c.6188T>A XP_011520683.1:p.Met2063Lys
XM_017022944.1:c.6935T>A XP_016878433.1:p.Met2312Lys
NM_004380.3:c.6941T>A MANE Select NP_004371.2:p.Met2314Lys