Canonical Allele Identifier: CA5672295
Gene: TAF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103383340T>C , CM000672.2:g.103383340T>C GRCh38
NC_000010.10:g.105143097T>C , CM000672.1:g.105143097T>C GRCh37
NC_000010.9:g.105133087T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000687501.1:n.3033T>C
ENST00000690052.1:c.*505T>C ENSP00000510708.1:n.*505T>C
ENST00000690667.1:n.1534+1499T>C
ENST00000692195.1:c.1637T>C ENSP00000510076.1:p.Val546Ala
ENST00000369839.4:c.1637T>C MANE Select ENSP00000358854.3:p.Val546Ala
ENST00000369839.3:c.1637T>C ENSP00000358854.3:p.Val546Ala
NM_006951.3:c.1637T>C NP_008882.2:p.Val546Ala
XM_011540108.1:c.1637T>C XP_011538410.1:p.Val546Ala
NM_006951.4:c.1637T>C NP_008882.2:p.Val546Ala
NM_139052.2:c.1637T>C NP_620640.1:p.Val546Ala
NM_006951.5:c.1637T>C MANE Select NP_008882.2:p.Val546Ala
NM_139052.3:c.1637T>C NP_620640.1:p.Val546Ala