Canonical Allele Identifier: CA2436448106
Gene: TAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71392681C= , CM000685.2:g.71392681C= GRCh38
NC_000023.10:g.70612531C= , CM000685.1:g.70612531C= GRCh37
NC_000023.9:g.70529256C= NCBI36
NG_012771.2:g.31418C=

Transcript Alleles

HGVS Amino-acid change
ENST00000276072.9:c.2180C= ENSP00000276072.5:p.Ser727=
ENST00000683202.1:c.2894C= ENSP00000507781.1:p.Ser965=
ENST00000683668.1:c.2180C= ENSP00000507280.1:p.Ser727=
ENST00000683715.1:c.2475C=
ENST00000683782.1:c.2894C= ENSP00000506996.1:p.Ser965=
ENST00000373790.9:c.2831C= ENSP00000362895.5:p.Ser944=
ENST00000423759.6:c.2894C= MANE Select ENSP00000406549.2:p.Ser965=
ENST00000276072.7:c.2954C= ENSP00000276072.3:p.Ser985=
ENST00000373790.8:c.2891C= ENSP00000362895.4:p.Ser964=
ENST00000423759.5:c.2954C= ENSP00000406549.1:p.Ser985=
NM_001286074.1:c.2954C= NP_001273003.1:p.Ser985=
NM_004606.4:c.2954C= NP_004597.2:p.Ser985=
NM_138923.3:c.2891C= NP_620278.1:p.Ser964=
NR_104387.1:n.3030C=
NR_104388.1:n.3030C=
NR_104389.1:n.3030C=
NR_104390.1:n.3030C=
NR_104391.1:n.3030C=
NR_104392.1:n.3030C=
NR_104393.1:n.3030C=
NR_104394.1:n.3030C=
NR_104395.1:n.3030C=
XM_005262295.1:c.2954C= XP_005262352.1:p.Ser985=
XM_005262296.1:c.2954C= XP_005262353.1:p.Ser985=
XM_005262297.3:c.2891C= XP_005262354.1:p.Ser964=
XM_005262300.1:c.2954C= XP_005262357.1:p.Ser985=
XM_006724682.2:c.2573C= XP_006724745.1:p.Ser858=
XM_011531016.1:c.2954C= XP_011529318.1:p.Ser985=
XR_938407.1:n.2964C=
XM_005262297.4:c.2891C= XP_005262354.1:p.Ser964=
XM_005262300.2:c.2954C= XP_005262357.1:p.Ser985=
XM_024452429.1:c.2573C= XP_024308197.1:p.Ser858=
XM_024452430.1:c.2954C= XP_024308198.1:p.Ser985=
NM_001286074.2:c.2894C= NP_001273003.2:p.Ser965=
NM_004606.5:c.2894C= MANE Select NP_004597.3:p.Ser965=
NM_138923.4:c.2831C= NP_620278.2:p.Ser944=
NR_104387.2:n.2912C=
NR_104388.2:n.2912C=
NR_104389.2:n.2912C=
NR_104390.2:n.2912C=
NR_104391.2:n.2912C=
NR_104392.2:n.2912C=
NR_104393.2:n.2912C=
NR_104394.2:n.2912C=
NR_104395.2:n.2912C=