Canonical Allele Identifier: CA1866632258

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675489G= , CM000671.2:g.97675489G=	GRCh38
NC_000009.11:g.100437771G= , CM000671.1:g.100437771G=	GRCh37
NC_000009.10:g.99477592G=	NCBI36
NG_011642.1:g.26921C= , LRG_471:g.26921C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.772C= MANE Select	ENSP00000364270.5:p.Arg258=
ENST00000375128.4:c.772C=	ENSP00000364270.4:p.Arg258=
ENST00000462523.5:c.*208C=	ENSP00000433006.1:n.*208C=
ENST00000485042.1:n.284C=
NM_000380.3:c.772C= , LRG_471t1:c.772C=	NP_000371.1:p.Arg258=
NR_027302.1:n.1120C=
XM_006717278.1:c.772C=	XP_006717341.1:p.Pro258=
XM_011518988.1:c.772C=	XP_011517290.1:p.Arg258=
NM_001354975.1:c.646C=	NP_001341904.1:p.Arg216=
NR_149091.1:n.617C=
NR_149092.1:n.783C=
NR_149093.1:n.1309C=
NR_149094.1:n.1203C=
NM_000380.4:c.772C= MANE Select	NP_000371.1:p.Arg258=
NM_001354975.2:c.646C=	NP_001341904.1:p.Arg216=
NR_027302.2:n.1051C=
NR_149091.2:n.548C=
NR_149092.2:n.714C=
NR_149093.2:n.1240C=
NR_149094.2:n.1134C=