Canonical Allele Identifier: CA1866632284

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675533T= , CM000671.2:g.97675533T=	GRCh38
NC_000009.11:g.100437815T= , CM000671.1:g.100437815T=	GRCh37
NC_000009.10:g.99477636T=	NCBI36
NG_011642.1:g.26877A= , LRG_471:g.26877A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.728A= MANE Select	ENSP00000364270.5:p.Gln243=
ENST00000375128.4:c.728A=	ENSP00000364270.4:p.Gln243=
ENST00000462523.5:c.*164A=	ENSP00000433006.1:n.*164A=
ENST00000485042.1:n.240A=
NM_000380.3:c.728A= , LRG_471t1:c.728A=	NP_000371.1:p.Gln243=
NR_027302.1:n.1076A=
XM_006717278.1:c.728A=	XP_006717341.1:p.Gln243=
XM_011518988.1:c.728A=	XP_011517290.1:p.Gln243=
XR_929839.1:n.1259A=
NM_001354975.1:c.602A=	NP_001341904.1:p.Gln201=
NR_149091.1:n.573A=
NR_149092.1:n.739A=
NR_149093.1:n.1265A=
NR_149094.1:n.1159A=
NM_000380.4:c.728A= MANE Select	NP_000371.1:p.Gln243=
NM_001354975.2:c.602A=	NP_001341904.1:p.Gln201=
NR_027302.2:n.1007A=
NR_149091.2:n.504A=
NR_149092.2:n.670A=
NR_149093.2:n.1196A=
NR_149094.2:n.1090A=