Canonical Allele Identifier: CA1866632183

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675353T= , CM000671.2:g.97675353T=	GRCh38
NC_000009.11:g.100437635T= , CM000671.1:g.100437635T=	GRCh37
NC_000009.10:g.99477456T=	NCBI36
NG_011642.1:g.27057A= , LRG_471:g.27057A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.*86A= MANE Select	ENSP00000364270.5:n.*86A=
ENST00000375128.4:c.*86A=	ENSP00000364270.4:n.*86A=
ENST00000462523.5:c.*344A=	ENSP00000433006.1:n.*344A=
ENST00000485042.1:n.420A=
NM_000380.3:c.*86A= , LRG_471t1:c.*86A=	NP_000371.1:n.*86A=
NR_027302.1:n.1256A=
XM_006717278.1:c.772+136A=	XP_006717341.1:n.772+136A=
XM_011518988.1:c.772+136A=	XP_011517290.1:n.772+136A=
NM_001354975.1:c.*86A=	NP_001341904.1:n.*86A=
NR_149091.1:n.753A=
NR_149092.1:n.919A=
NR_149093.1:n.1445A=
NR_149094.1:n.1339A=
NM_000380.4:c.*86A= MANE Select	NP_000371.1:n.*86A=
NM_001354975.2:c.*86A=	NP_001341904.1:n.*86A=
NR_027302.2:n.1187A=
NR_149091.2:n.684A=
NR_149092.2:n.850A=
NR_149093.2:n.1376A=
NR_149094.2:n.1270A=