Canonical Allele Identifier: CA1866632287

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675540C= , CM000671.2:g.97675540C=	GRCh38
NC_000009.11:g.100437822C= , CM000671.1:g.100437822C=	GRCh37
NC_000009.10:g.99477643C=	NCBI36
NG_011642.1:g.26870G= , LRG_471:g.26870G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.721G= MANE Select	ENSP00000364270.5:p.Val241=
ENST00000375128.4:c.721G=	ENSP00000364270.4:p.Val241=
ENST00000462523.5:c.*157G=	ENSP00000433006.1:n.*157G=
ENST00000485042.1:n.233G=
NM_000380.3:c.721G= , LRG_471t1:c.721G=	NP_000371.1:p.Val241=
NR_027302.1:n.1069G=
XM_006717278.1:c.721G=	XP_006717341.1:p.Val241=
XM_011518988.1:c.721G=	XP_011517290.1:p.Val241=
XR_929839.1:n.1252G=
NM_001354975.1:c.595G=	NP_001341904.1:p.Val199=
NR_149091.1:n.566G=
NR_149092.1:n.732G=
NR_149093.1:n.1258G=
NR_149094.1:n.1152G=
NM_000380.4:c.721G= MANE Select	NP_000371.1:p.Val241=
NM_001354975.2:c.595G=	NP_001341904.1:p.Val199=
NR_027302.2:n.1000G=
NR_149091.2:n.497G=
NR_149092.2:n.663G=
NR_149093.2:n.1189G=
NR_149094.2:n.1083G=