Canonical Allele Identifier: CA5148803

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97687088T>C , CM000671.2:g.97687088T>C	GRCh38
NC_000009.11:g.100449370T>C , CM000671.1:g.100449370T>C	GRCh37
NC_000009.10:g.99489191T>C	NCBI36
NG_011642.1:g.15322A>G , LRG_471:g.15322A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000380.4:c.555+8A>G MANE Select	NP_000371.1:n.555+8A>G
ENST00000375128.5:c.555+8A>G MANE Select	ENSP00000364270.5:n.555+8A>G
NM_000380.3:c.555+8A>G , LRG_471t1:c.555+8A>G	NP_000371.1:n.555+8A>G
NM_001354975.1:c.429+8A>G	NP_001341904.1:n.429+8A>G
NM_001354975.2:c.429+8A>G	NP_001341904.1:n.429+8A>G
NR_027302.1:n.672+8A>G
NR_027302.2:n.603+8A>G
NR_149091.1:n.401-2048A>G
NR_149091.2:n.332-2048A>G
NR_149092.1:n.566+8A>G
NR_149092.2:n.497+8A>G
NR_149093.1:n.672+8A>G
NR_149093.2:n.603+8A>G
NR_149094.1:n.566+8A>G
NR_149094.2:n.497+8A>G
ENST00000375128.4:c.555+8A>G	ENSP00000364270.4:n.555+8A>G
ENST00000462523.5:c.555+8A>G	ENSP00000433006.1:n.555+8A>G
ENST00000496104.1:n.349+8A>G
XM_006717278.1:c.555+8A>G	XP_006717341.1:n.555+8A>G
XM_011518988.1:c.555+8A>G	XP_011517290.1:n.555+8A>G
XR_929839.1:n.666+8A>G