Canonical Allele Identifier: CA1866632428

Gene: XPA

Linked Data

• dbSNP Id: rs1828345674

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675766C>T , CM000671.2:g.97675766C>T	GRCh38
NC_000009.11:g.100438048C>T , CM000671.1:g.100438048C>T	GRCh37
NC_000009.10:g.99477869C>T	NCBI36
NG_011642.1:g.26644G>A , LRG_471:g.26644G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-179G>A MANE Select	ENSP00000364270.5:n.674-179G>A
ENST00000375128.4:c.674-179G>A	ENSP00000364270.4:n.674-179G>A
ENST00000462523.5:c.*110-179G>A	ENSP00000433006.1:n.*110-179G>A
ENST00000485042.1:n.185+5G>A
NM_000380.3:c.674-179G>A , LRG_471t1:c.674-179G>A	NP_000371.1:n.674-179G>A
NR_027302.1:n.1022-179G>A
XM_006717278.1:c.674-179G>A	XP_006717341.1:n.674-179G>A
XM_011518988.1:c.674-179G>A	XP_011517290.1:n.674-179G>A
XR_929839.1:n.1204+5G>A
NM_001354975.1:c.548-179G>A	NP_001341904.1:n.548-179G>A
NR_149091.1:n.519-179G>A
NR_149092.1:n.685-179G>A
NR_149093.1:n.1210+5G>A
NR_149094.1:n.1104+5G>A
NM_000380.4:c.674-179G>A MANE Select	NP_000371.1:n.674-179G>A
NM_001354975.2:c.548-179G>A	NP_001341904.1:n.548-179G>A
NR_027302.2:n.953-179G>A
NR_149091.2:n.450-179G>A
NR_149092.2:n.616-179G>A
NR_149093.2:n.1141+5G>A
NR_149094.2:n.1035+5G>A