Canonical Allele Identifier: CA374185481

Gene: XPA

Linked Data

• MyVariant Identifiers: chr9:g.100437829C>G (hg19) ; chr9:g.97675547C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675547C>G , CM000671.2:g.97675547C>G	GRCh38
NC_000009.11:g.100437829C>G , CM000671.1:g.100437829C>G	GRCh37
NC_000009.10:g.99477650C>G	NCBI36
NG_011642.1:g.26863G>C , LRG_471:g.26863G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.714G>C MANE Select	ENSP00000364270.5:p.Glu238Asp
ENST00000375128.4:c.714G>C	ENSP00000364270.4:p.Glu238Asp
ENST00000462523.5:c.*150G>C	ENSP00000433006.1:n.*150G>C
ENST00000485042.1:n.226G>C
NM_000380.3:c.714G>C , LRG_471t1:c.714G>C	NP_000371.1:p.Glu238Asp
NR_027302.1:n.1062G>C
XM_006717278.1:c.714G>C	XP_006717341.1:p.Glu238Asp
XM_011518988.1:c.714G>C	XP_011517290.1:p.Glu238Asp
XR_929839.1:n.1245G>C
NM_001354975.1:c.588G>C	NP_001341904.1:p.Glu196Asp
NR_149091.1:n.559G>C
NR_149092.1:n.725G>C
NR_149093.1:n.1251G>C
NR_149094.1:n.1145G>C
NM_000380.4:c.714G>C MANE Select	NP_000371.1:p.Glu238Asp
NM_001354975.2:c.588G>C	NP_001341904.1:p.Glu196Asp
NR_027302.2:n.993G>C
NR_149091.2:n.490G>C
NR_149092.2:n.656G>C
NR_149093.2:n.1182G>C
NR_149094.2:n.1076G>C