Canonical Allele Identifier: CA1866632459

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675813G= , CM000671.2:g.97675813G=	GRCh38
NC_000009.11:g.100438095G= , CM000671.1:g.100438095G=	GRCh37
NC_000009.10:g.99477916G=	NCBI36
NG_011642.1:g.26597C= , LRG_471:g.26597C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-226C= MANE Select	ENSP00000364270.5:n.674-226C=
ENST00000375128.4:c.674-226C=	ENSP00000364270.4:n.674-226C=
ENST00000462523.5:c.*110-226C=	ENSP00000433006.1:n.*110-226C=
ENST00000485042.1:n.143C=
NM_000380.3:c.674-226C= , LRG_471t1:c.674-226C=	NP_000371.1:n.674-226C=
NR_027302.1:n.1022-226C=
XM_006717278.1:c.674-226C=	XP_006717341.1:n.674-226C=
XM_011518988.1:c.674-226C=	XP_011517290.1:n.674-226C=
XR_929839.1:n.1162C=
NM_001354975.1:c.548-226C=	NP_001341904.1:n.548-226C=
NR_149091.1:n.519-226C=
NR_149092.1:n.685-226C=
NR_149093.1:n.1168C=
NR_149094.1:n.1062C=
NM_000380.4:c.674-226C= MANE Select	NP_000371.1:n.674-226C=
NM_001354975.2:c.548-226C=	NP_001341904.1:n.548-226C=
NR_027302.2:n.953-226C=
NR_149091.2:n.450-226C=
NR_149092.2:n.616-226C=
NR_149093.2:n.1099C=
NR_149094.2:n.993C=