Canonical Allele Identifier: CA377982060
Gene: TAF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103381740T>A , CM000672.2:g.103381740T>A GRCh38
NC_000010.10:g.105141497T>A , CM000672.1:g.105141497T>A GRCh37
NC_000010.9:g.105131487T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000687501.1:n.1433T>A
ENST00000690052.1:c.*301T>A ENSP00000510708.1:n.*301T>A
ENST00000690667.1:n.1433T>A
ENST00000692195.1:c.1433T>A ENSP00000510076.1:p.Val478Asp
ENST00000369839.4:c.1433T>A MANE Select ENSP00000358854.3:p.Val478Asp
ENST00000369839.3:c.1433T>A ENSP00000358854.3:p.Val478Asp
NM_006951.3:c.1433T>A NP_008882.2:p.Val478Asp
XM_011540108.1:c.1433T>A XP_011538410.1:p.Val478Asp
NM_006951.4:c.1433T>A NP_008882.2:p.Val478Asp
NM_139052.2:c.1433T>A NP_620640.1:p.Val478Asp
NM_006951.5:c.1433T>A MANE Select NP_008882.2:p.Val478Asp
NM_139052.3:c.1433T>A NP_620640.1:p.Val478Asp