Canonical Allele Identifier: CA374185518

Gene: XPA

Linked Data

• MyVariant Identifiers: chr9:g.100437845C>A (hg19) ; chr9:g.97675563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675563C>A , CM000671.2:g.97675563C>A	GRCh38
NC_000009.11:g.100437845C>A , CM000671.1:g.100437845C>A	GRCh37
NC_000009.10:g.99477666C>A	NCBI36
NG_011642.1:g.26847G>T , LRG_471:g.26847G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.698G>T MANE Select	ENSP00000364270.5:p.Ser233Ile
ENST00000375128.4:c.698G>T	ENSP00000364270.4:p.Ser233Ile
ENST00000462523.5:c.*134G>T	ENSP00000433006.1:n.*134G>T
ENST00000485042.1:n.210G>T
NM_000380.3:c.698G>T , LRG_471t1:c.698G>T	NP_000371.1:p.Ser233Ile
NR_027302.1:n.1046G>T
XM_006717278.1:c.698G>T	XP_006717341.1:p.Ser233Ile
XM_011518988.1:c.698G>T	XP_011517290.1:p.Ser233Ile
XR_929839.1:n.1229G>T
NM_001354975.1:c.572G>T	NP_001341904.1:p.Ser191Ile
NR_149091.1:n.543G>T
NR_149092.1:n.709G>T
NR_149093.1:n.1235G>T
NR_149094.1:n.1129G>T
NM_000380.4:c.698G>T MANE Select	NP_000371.1:p.Ser233Ile
NM_001354975.2:c.572G>T	NP_001341904.1:p.Ser191Ile
NR_027302.2:n.977G>T
NR_149091.2:n.474G>T
NR_149092.2:n.640G>T
NR_149093.2:n.1166G>T
NR_149094.2:n.1060G>T