Canonical Allele Identifier: CA1866632405

Gene: XPA

Linked Data

• dbSNP Id: rs1828343625

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675711A>T , CM000671.2:g.97675711A>T	GRCh38
NC_000009.11:g.100437993A>T , CM000671.1:g.100437993A>T	GRCh37
NC_000009.10:g.99477814A>T	NCBI36
NG_011642.1:g.26699T>A , LRG_471:g.26699T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-124T>A MANE Select	ENSP00000364270.5:n.674-124T>A
ENST00000375128.4:c.674-124T>A	ENSP00000364270.4:n.674-124T>A
ENST00000462523.5:c.*110-124T>A	ENSP00000433006.1:n.*110-124T>A
ENST00000485042.1:n.185+60T>A
NM_000380.3:c.674-124T>A , LRG_471t1:c.674-124T>A	NP_000371.1:n.674-124T>A
NR_027302.1:n.1022-124T>A
XM_006717278.1:c.674-124T>A	XP_006717341.1:n.674-124T>A
XM_011518988.1:c.674-124T>A	XP_011517290.1:n.674-124T>A
XR_929839.1:n.1204+60T>A
NM_001354975.1:c.548-124T>A	NP_001341904.1:n.548-124T>A
NR_149091.1:n.519-124T>A
NR_149092.1:n.685-124T>A
NR_149093.1:n.1210+60T>A
NR_149094.1:n.1104+60T>A
NM_000380.4:c.674-124T>A MANE Select	NP_000371.1:n.674-124T>A
NM_001354975.2:c.548-124T>A	NP_001341904.1:n.548-124T>A
NR_027302.2:n.953-124T>A
NR_149091.2:n.450-124T>A
NR_149092.2:n.616-124T>A
NR_149093.2:n.1141+60T>A
NR_149094.2:n.1035+60T>A