Canonical Allele Identifier: CA2631399163
Gene: CREBBP HGNC NCBI

Linked Data

gnomAD v4: 16-3729914-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729914G>T , CM000678.2:g.3729914G>T GRCh38
NC_000016.9:g.3779915G>T , CM000678.1:g.3779915G>T GRCh37
NC_000016.8:g.3719916G>T NCBI36
NG_009873.1:g.155207C>A
NG_009873.2:g.155800C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5173-40C>A MANE Select ENSP00000262367.5:n.5173-40C>A
ENST00000262367.9:c.5173-40C>A ENSP00000262367.5:n.5173-40C>A
ENST00000382070.7:c.5059-40C>A ENSP00000371502.3:n.5059-40C>A
NM_001079846.1:c.5059-40C>A NP_001073315.1:n.5059-40C>A
NM_004380.2:c.5173-40C>A NP_004371.2:n.5173-40C>A
XM_005255124.3:c.5128-40C>A XP_005255181.1:n.5128-40C>A
XM_005255125.3:c.4756-40C>A XP_005255182.1:n.4756-40C>A
XM_006720848.2:c.4912-40C>A XP_006720911.1:n.4912-40C>A
XM_011522380.1:c.5119-40C>A XP_011520682.1:n.5119-40C>A
XM_011522381.1:c.4420-40C>A XP_011520683.1:n.4420-40C>A
XM_005255124.4:c.5128-40C>A XP_005255181.1:n.5128-40C>A
XM_005255125.4:c.4756-40C>A XP_005255182.1:n.4756-40C>A
XM_006720848.3:c.4912-40C>A XP_006720911.1:n.4912-40C>A
XM_011522381.2:c.4420-40C>A XP_011520683.1:n.4420-40C>A
XM_017022944.1:c.5167-40C>A XP_016878433.1:n.5167-40C>A
NM_004380.3:c.5173-40C>A MANE Select NP_004371.2:n.5173-40C>A