Canonical Allele Identifier: CA1866632303

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675574T= , CM000671.2:g.97675574T=	GRCh38
NC_000009.11:g.100437856T= , CM000671.1:g.100437856T=	GRCh37
NC_000009.10:g.99477677T=	NCBI36
NG_011642.1:g.26836A= , LRG_471:g.26836A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.687A= MANE Select	ENSP00000364270.5:p.Ala229=
ENST00000375128.4:c.687A=	ENSP00000364270.4:p.Ala229=
ENST00000462523.5:c.*123A=	ENSP00000433006.1:n.*123A=
ENST00000485042.1:n.199A=
NM_000380.3:c.687A= , LRG_471t1:c.687A=	NP_000371.1:p.Ala229=
NR_027302.1:n.1035A=
XM_006717278.1:c.687A=	XP_006717341.1:p.Ala229=
XM_011518988.1:c.687A=	XP_011517290.1:p.Ala229=
XR_929839.1:n.1218A=
NM_001354975.1:c.561A=	NP_001341904.1:p.Ala187=
NR_149091.1:n.532A=
NR_149092.1:n.698A=
NR_149093.1:n.1224A=
NR_149094.1:n.1118A=
NM_000380.4:c.687A= MANE Select	NP_000371.1:p.Ala229=
NM_001354975.2:c.561A=	NP_001341904.1:p.Ala187=
NR_027302.2:n.966A=
NR_149091.2:n.463A=
NR_149092.2:n.629A=
NR_149093.2:n.1155A=
NR_149094.2:n.1049A=