Canonical Allele Identifier: CA1866632415

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675735G= , CM000671.2:g.97675735G=	GRCh38
NC_000009.11:g.100438017G= , CM000671.1:g.100438017G=	GRCh37
NC_000009.10:g.99477838G=	NCBI36
NG_011642.1:g.26675C= , LRG_471:g.26675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-148C= MANE Select	ENSP00000364270.5:n.674-148C=
ENST00000375128.4:c.674-148C=	ENSP00000364270.4:n.674-148C=
ENST00000462523.5:c.*110-148C=	ENSP00000433006.1:n.*110-148C=
ENST00000485042.1:n.185+36C=
NM_000380.3:c.674-148C= , LRG_471t1:c.674-148C=	NP_000371.1:n.674-148C=
NR_027302.1:n.1022-148C=
XM_006717278.1:c.674-148C=	XP_006717341.1:n.674-148C=
XM_011518988.1:c.674-148C=	XP_011517290.1:n.674-148C=
XR_929839.1:n.1204+36C=
NM_001354975.1:c.548-148C=	NP_001341904.1:n.548-148C=
NR_149091.1:n.519-148C=
NR_149092.1:n.685-148C=
NR_149093.1:n.1210+36C=
NR_149094.1:n.1104+36C=
NM_000380.4:c.674-148C= MANE Select	NP_000371.1:n.674-148C=
NM_001354975.2:c.548-148C=	NP_001341904.1:n.548-148C=
NR_027302.2:n.953-148C=
NR_149091.2:n.450-148C=
NR_149092.2:n.616-148C=
NR_149093.2:n.1141+36C=
NR_149094.2:n.1035+36C=