Canonical Allele Identifier: CA2575893819
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729900C>A , CM000678.2:g.3729900C>A GRCh38
NC_000016.9:g.3779901C>A , CM000678.1:g.3779901C>A GRCh37
NC_000016.8:g.3719902C>A NCBI36
NG_009873.1:g.155221G>T
NG_009873.2:g.155814G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5173-26G>T MANE Select ENSP00000262367.5:n.5173-26G>T
ENST00000262367.9:c.5173-26G>T ENSP00000262367.5:n.5173-26G>T
ENST00000382070.7:c.5059-26G>T ENSP00000371502.3:n.5059-26G>T
NM_001079846.1:c.5059-26G>T NP_001073315.1:n.5059-26G>T
NM_004380.2:c.5173-26G>T NP_004371.2:n.5173-26G>T
XM_005255124.3:c.5128-26G>T XP_005255181.1:n.5128-26G>T
XM_005255125.3:c.4756-26G>T XP_005255182.1:n.4756-26G>T
XM_006720848.2:c.4912-26G>T XP_006720911.1:n.4912-26G>T
XM_011522380.1:c.5119-26G>T XP_011520682.1:n.5119-26G>T
XM_011522381.1:c.4420-26G>T XP_011520683.1:n.4420-26G>T
XM_005255124.4:c.5128-26G>T XP_005255181.1:n.5128-26G>T
XM_005255125.4:c.4756-26G>T XP_005255182.1:n.4756-26G>T
XM_006720848.3:c.4912-26G>T XP_006720911.1:n.4912-26G>T
XM_011522381.2:c.4420-26G>T XP_011520683.1:n.4420-26G>T
XM_017022944.1:c.5167-26G>T XP_016878433.1:n.5167-26G>T
NM_004380.3:c.5173-26G>T MANE Select NP_004371.2:n.5173-26G>T