Canonical Allele Identifier: CA1866632445

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675793C= , CM000671.2:g.97675793C=	GRCh38
NC_000009.11:g.100438075C= , CM000671.1:g.100438075C=	GRCh37
NC_000009.10:g.99477896C=	NCBI36
NG_011642.1:g.26617G= , LRG_471:g.26617G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-206G= MANE Select	ENSP00000364270.5:n.674-206G=
ENST00000375128.4:c.674-206G=	ENSP00000364270.4:n.674-206G=
ENST00000462523.5:c.*110-206G=	ENSP00000433006.1:n.*110-206G=
ENST00000485042.1:n.163G=
NM_000380.3:c.674-206G= , LRG_471t1:c.674-206G=	NP_000371.1:n.674-206G=
NR_027302.1:n.1022-206G=
XM_006717278.1:c.674-206G=	XP_006717341.1:n.674-206G=
XM_011518988.1:c.674-206G=	XP_011517290.1:n.674-206G=
XR_929839.1:n.1182G=
NM_001354975.1:c.548-206G=	NP_001341904.1:n.548-206G=
NR_149091.1:n.519-206G=
NR_149092.1:n.685-206G=
NR_149093.1:n.1188G=
NR_149094.1:n.1082G=
NM_000380.4:c.674-206G= MANE Select	NP_000371.1:n.674-206G=
NM_001354975.2:c.548-206G=	NP_001341904.1:n.548-206G=
NR_027302.2:n.953-206G=
NR_149091.2:n.450-206G=
NR_149092.2:n.616-206G=
NR_149093.2:n.1119G=
NR_149094.2:n.1013G=