Canonical Allele Identifier: CA413533255
Community Standard Title: NM_004606.5(TAF1):c.3796G>C (p.Gly1266Arg)
Gene: TAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71401537G>C , CM000685.2:g.71401537G>C GRCh38
NC_000023.10:g.70621387G>C , CM000685.1:g.70621387G>C GRCh37
NC_000023.9:g.70538112G>C NCBI36
NG_012771.2:g.40274G>C

Transcript Alleles

HGVS Amino-acid Change
NM_004606.5:c.3796G>C MANE Select NP_004597.3:p.Gly1266Arg
ENST00000423759.6:c.3796G>C MANE Select ENSP00000406549.2:p.Gly1266Arg
NM_001286074.1:c.3856G>C NP_001273003.1:p.Gly1286Arg
NM_001286074.2:c.3796G>C NP_001273003.2:p.Gly1266Arg
NM_004606.4:c.3856G>C NP_004597.2:p.Gly1286Arg
NM_138923.3:c.3793G>C NP_620278.1:p.Gly1265Arg
NM_138923.4:c.3733G>C NP_620278.2:p.Gly1245Arg
NR_104387.1:n.3932G>C
NR_104387.2:n.3814G>C
NR_104388.1:n.3932G>C
NR_104388.2:n.3814G>C
NR_104389.1:n.3932G>C
NR_104389.2:n.3814G>C
NR_104390.1:n.3932G>C
NR_104390.2:n.3814G>C
NR_104391.1:n.3932G>C
NR_104391.2:n.3814G>C
NR_104392.1:n.3932G>C
NR_104392.2:n.3814G>C
NR_104393.1:n.3932G>C
NR_104393.2:n.3814G>C
NR_104394.1:n.3932G>C
NR_104394.2:n.3814G>C
NR_104395.1:n.3932G>C
NR_104395.2:n.3814G>C
ENST00000276072.7:c.3856G>C ENSP00000276072.3:p.Gly1286Arg
ENST00000276072.8:c.390G>C
ENST00000276072.9:c.3082G>C ENSP00000276072.5:p.Gly1028Arg
ENST00000373790.8:c.3793G>C ENSP00000362895.4:p.Gly1265Arg
ENST00000373790.9:c.3733G>C ENSP00000362895.5:p.Gly1245Arg
ENST00000423759.5:c.3856G>C ENSP00000406549.1:p.Gly1286Arg
ENST00000483985.2:c.525G>C
ENST00000483985.3:c.711G>C
ENST00000683202.1:c.3796G>C ENSP00000507781.1:p.Gly1266Arg
ENST00000683668.1:c.3082G>C ENSP00000507280.1:p.Gly1028Arg
ENST00000683782.1:c.3796G>C ENSP00000506996.1:p.Gly1266Arg
XM_005262295.1:c.3856G>C XP_005262352.1:p.Gly1286Arg
XM_005262296.1:c.3853G>C XP_005262353.1:p.Gly1285Arg
XM_005262297.3:c.3793G>C XP_005262354.1:p.Gly1265Arg
XM_005262297.4:c.3793G>C XP_005262354.1:p.Gly1265Arg
XM_006724682.2:c.3475G>C XP_006724745.1:p.Gly1159Arg
XM_011531016.1:c.3856G>C XP_011529318.1:p.Gly1286Arg
XM_024452429.1:c.3475G>C XP_024308197.1:p.Gly1159Arg
XM_024452430.1:c.3856G>C XP_024308198.1:p.Gly1286Arg
XR_938407.1:n.3866G>C