Canonical Allele Identifier: CA374188340

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97697120C>T , CM000671.2:g.97697120C>T	GRCh38
NC_000009.11:g.100459402C>T , CM000671.1:g.100459402C>T	GRCh37
NC_000009.10:g.99499223C>T	NCBI36
NG_011642.1:g.5290G>A , LRG_471:g.5290G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000380.4:c.172+1G>A MANE Select	NP_000371.1:n.172+1G>A
ENST00000375128.5:c.172+1G>A MANE Select	ENSP00000364270.5:n.172+1G>A
NM_000380.3:c.172+1G>A , LRG_471t1:c.172+1G>A	NP_000371.1:n.172+1G>A
NM_001354975.1:c.-977G>A	NP_001341904.1:n.-977G>A
NM_001354975.2:c.-977G>A	NP_001341904.1:n.-977G>A
NR_027302.1:n.289+1G>A
NR_027302.2:n.220+1G>A
NR_149091.1:n.289+1G>A
NR_149091.2:n.220+1G>A
NR_149092.1:n.289+1G>A
NR_149092.2:n.220+1G>A
NR_149093.1:n.289+1G>A
NR_149093.2:n.220+1G>A
NR_149094.1:n.289+1G>A
NR_149094.2:n.220+1G>A
ENST00000375128.4:c.172+1G>A	ENSP00000364270.4:n.172+1G>A
ENST00000462523.5:c.172+1G>A	ENSP00000433006.1:n.172+1G>A
ENST00000496104.1:n.72+104G>A
XM_006717278.1:c.172+1G>A	XP_006717341.1:n.172+1G>A
XM_011518988.1:c.172+1G>A	XP_011517290.1:n.172+1G>A
XR_929839.1:n.283+1G>A