Canonical Allele Identifier: CA394551535
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2141203055

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770853A>C , CM000678.2:g.3770853A>C GRCh38
NC_000016.9:g.3820854A>C , CM000678.1:g.3820854A>C GRCh37
NC_000016.8:g.3760855A>C NCBI36
NG_009873.1:g.114268T>G
NG_009873.2:g.114861T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2597T>G MANE Select ENSP00000262367.5:p.Met866Arg
ENST00000262367.9:c.2597T>G ENSP00000262367.5:p.Met866Arg
ENST00000382070.7:c.2483T>G ENSP00000371502.3:p.Met828Arg
ENST00000570939.2:c.1202T>G ENSP00000461002.2:p.Met401Arg
NM_001079846.1:c.2483T>G NP_001073315.1:p.Met828Arg
NM_004380.2:c.2597T>G NP_004371.2:p.Met866Arg
XM_005255124.3:c.2552T>G XP_005255181.1:p.Met851Arg
XM_005255125.3:c.2464-1500T>G XP_005255182.1:n.2464-1500T>G
XM_006720848.2:c.2597T>G XP_006720911.1:p.Met866Arg
XM_011522380.1:c.2543T>G XP_011520682.1:p.Met848Arg
XM_011522381.1:c.1844T>G XP_011520683.1:p.Met615Arg
XM_011522382.1:c.2597T>G XP_011520684.1:p.Met866Arg
XM_005255124.4:c.2552T>G XP_005255181.1:p.Met851Arg
XM_005255125.4:c.2464-1500T>G XP_005255182.1:n.2464-1500T>G
XM_006720848.3:c.2597T>G XP_006720911.1:p.Met866Arg
XM_011522381.2:c.1844T>G XP_011520683.1:p.Met615Arg
XM_011522382.3:c.2597T>G XP_011520684.1:p.Met866Arg
XM_017022944.1:c.2591T>G XP_016878433.1:p.Met864Arg
NM_004380.3:c.2597T>G MANE Select NP_004371.2:p.Met866Arg