Canonical Allele Identifier: CA5672254
Gene: TAF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103381735G>C , CM000672.2:g.103381735G>C GRCh38
NC_000010.10:g.105141492G>C , CM000672.1:g.105141492G>C GRCh37
NC_000010.9:g.105131482G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006951.5:c.1428G>C MANE Select NP_008882.2:p.Val476=
ENST00000369839.4:c.1428G>C MANE Select ENSP00000358854.3:p.Val476=
NM_006951.3:c.1428G>C NP_008882.2:p.Val476=
NM_006951.4:c.1428G>C NP_008882.2:p.Val476=
NM_139052.2:c.1428G>C NP_620640.1:p.Val476=
NM_139052.3:c.1428G>C NP_620640.1:p.Val476=
ENST00000369839.3:c.1428G>C ENSP00000358854.3:p.Val476=
ENST00000687501.1:n.1428G>C
ENST00000690052.1:c.*296G>C ENSP00000510708.1:n.*296G>C
ENST00000690667.1:n.1428G>C
ENST00000692195.1:c.1428G>C ENSP00000510076.1:p.Val476=
XM_011540108.1:c.1428G>C XP_011538410.1:p.Val476=