Canonical Allele Identifier: CA1866632291

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675545G= , CM000671.2:g.97675545G=	GRCh38
NC_000009.11:g.100437827G= , CM000671.1:g.100437827G=	GRCh37
NC_000009.10:g.99477648G=	NCBI36
NG_011642.1:g.26865C= , LRG_471:g.26865C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.716C= MANE Select	ENSP00000364270.5:p.Thr239=
ENST00000375128.4:c.716C=	ENSP00000364270.4:p.Thr239=
ENST00000462523.5:c.*152C=	ENSP00000433006.1:n.*152C=
ENST00000485042.1:n.228C=
NM_000380.3:c.716C= , LRG_471t1:c.716C=	NP_000371.1:p.Thr239=
NR_027302.1:n.1064C=
XM_006717278.1:c.716C=	XP_006717341.1:p.Thr239=
XM_011518988.1:c.716C=	XP_011517290.1:p.Thr239=
XR_929839.1:n.1247C=
NM_001354975.1:c.590C=	NP_001341904.1:p.Thr197=
NR_149091.1:n.561C=
NR_149092.1:n.727C=
NR_149093.1:n.1253C=
NR_149094.1:n.1147C=
NM_000380.4:c.716C= MANE Select	NP_000371.1:p.Thr239=
NM_001354975.2:c.590C=	NP_001341904.1:p.Thr197=
NR_027302.2:n.995C=
NR_149091.2:n.492C=
NR_149092.2:n.658C=
NR_149093.2:n.1184C=
NR_149094.2:n.1078C=