Canonical Allele Identifier: CA3804511

Gene: TAF8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42050591G>A , CM000668.2:g.42050591G>A	GRCh38
NC_000006.11:g.42018329G>A , CM000668.1:g.42018329G>A	GRCh37
NC_000006.10:g.42126307G>A	NCBI36
NG_041939.1:g.3304C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138572.3:c.45+5G>A MANE Select	NP_612639.2:n.45+5G>A
ENST00000372977.8:c.45+5G>A MANE Select	ENSP00000362068.3:n.45+5G>A
NM_138572.2:c.45+5G>A	NP_612639.2:n.45+5G>A
ENST00000372977.7:c.45+5G>A	ENSP00000362068.3:n.45+5G>A
ENST00000372978.7:c.45+5G>A	ENSP00000362069.3:n.45+5G>A
ENST00000372982.8:c.45+5G>A	ENSP00000362073.4:n.45+5G>A
ENST00000456846.6:c.45+5G>A	ENSP00000411900.2:n.45+5G>A
ENST00000472818.5:c.45+5G>A	ENSP00000417760.1:n.45+5G>A
ENST00000472818.6:n.68G>A
ENST00000482926.1:n.48+5G>A
ENST00000486070.1:n.56+5G>A
ENST00000494547.5:c.45+5G>A	ENSP00000417867.1:n.45+5G>A
ENST00000686229.1:c.45+5G>A	ENSP00000510786.1:n.45+5G>A
ENST00000686935.1:c.45+5G>A	ENSP00000509629.1:n.45+5G>A
ENST00000687601.1:c.45+5G>A	ENSP00000510369.1:n.45+5G>A
ENST00000688007.1:c.45+5G>A	ENSP00000509560.1:n.45+5G>A
ENST00000688562.1:n.63+5G>A
ENST00000689833.1:n.53+5G>A
ENST00000691805.1:n.63+5G>A
XM_005248849.2:c.45+5G>A	XP_005248906.1:n.45+5G>A
XM_011514296.1:c.45+5G>A	XP_011512598.1:n.45+5G>A
XM_011514296.2:c.45+5G>A	XP_011512598.1:n.45+5G>A
XM_011514297.1:c.45+5G>A	XP_011512599.1:n.45+5G>A
XM_017010241.2:c.45+5G>A	XP_016865730.1:n.45+5G>A
XM_017010244.2:c.45+5G>A	XP_016865733.1:n.45+5G>A
XM_017010245.1:c.45+5G>A	XP_016865734.1:n.45+5G>A