Canonical Allele Identifier: CA1866632282

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675528C= , CM000671.2:g.97675528C=	GRCh38
NC_000009.11:g.100437810C= , CM000671.1:g.100437810C=	GRCh37
NC_000009.10:g.99477631C=	NCBI36
NG_011642.1:g.26882G= , LRG_471:g.26882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.733G= MANE Select	ENSP00000364270.5:p.Glu245=
ENST00000375128.4:c.733G=	ENSP00000364270.4:p.Glu245=
ENST00000462523.5:c.*169G=	ENSP00000433006.1:n.*169G=
ENST00000485042.1:n.245G=
NM_000380.3:c.733G= , LRG_471t1:c.733G=	NP_000371.1:p.Glu245=
NR_027302.1:n.1081G=
XM_006717278.1:c.733G=	XP_006717341.1:p.Glu245=
XM_011518988.1:c.733G=	XP_011517290.1:p.Glu245=
XR_929839.1:n.1264G=
NM_001354975.1:c.607G=	NP_001341904.1:p.Glu203=
NR_149091.1:n.578G=
NR_149092.1:n.744G=
NR_149093.1:n.1270G=
NR_149094.1:n.1164G=
NM_000380.4:c.733G= MANE Select	NP_000371.1:p.Glu245=
NM_001354975.2:c.607G=	NP_001341904.1:p.Glu203=
NR_027302.2:n.1012G=
NR_149091.2:n.509G=
NR_149092.2:n.675G=
NR_149093.2:n.1201G=
NR_149094.2:n.1095G=