Canonical Allele Identifier: CA374185386

Gene: XPA

Linked Data

• gnomAD v4: 9-97675504-C-A
• MyVariant Identifiers: chr9:g.100437786C>A (hg19) ; chr9:g.97675504C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675504C>A , CM000671.2:g.97675504C>A	GRCh38
NC_000009.11:g.100437786C>A , CM000671.1:g.100437786C>A	GRCh37
NC_000009.10:g.99477607C>A	NCBI36
NG_011642.1:g.26906G>T , LRG_471:g.26906G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.757G>T MANE Select	ENSP00000364270.5:p.Glu253Ter
ENST00000375128.4:c.757G>T	ENSP00000364270.4:p.Glu253Ter
ENST00000462523.5:c.*193G>T	ENSP00000433006.1:n.*193G>T
ENST00000485042.1:n.269G>T
NM_000380.3:c.757G>T , LRG_471t1:c.757G>T	NP_000371.1:p.Glu253Ter
NR_027302.1:n.1105G>T
XM_006717278.1:c.757G>T	XP_006717341.1:p.Glu253Ter
XM_011518988.1:c.757G>T	XP_011517290.1:p.Glu253Ter
XR_929839.1:n.1288G>T
NM_001354975.1:c.631G>T	NP_001341904.1:p.Glu211Ter
NR_149091.1:n.602G>T
NR_149092.1:n.768G>T
NR_149093.1:n.1294G>T
NR_149094.1:n.1188G>T
NM_000380.4:c.757G>T MANE Select	NP_000371.1:p.Glu253Ter
NM_001354975.2:c.631G>T	NP_001341904.1:p.Glu211Ter
NR_027302.2:n.1036G>T
NR_149091.2:n.533G>T
NR_149092.2:n.699G>T
NR_149093.2:n.1225G>T
NR_149094.2:n.1119G>T