Canonical Allele Identifier: CA2690901807

Gene: XPA

Linked Data

• gnomAD v4: 9-97675806-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675806G>A , CM000671.2:g.97675806G>A	GRCh38
NC_000009.11:g.100438088G>A , CM000671.1:g.100438088G>A	GRCh37
NC_000009.10:g.99477909G>A	NCBI36
NG_011642.1:g.26604C>T , LRG_471:g.26604C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-219C>T MANE Select	ENSP00000364270.5:n.674-219C>T
ENST00000375128.4:c.674-219C>T	ENSP00000364270.4:n.674-219C>T
ENST00000462523.5:c.*110-219C>T	ENSP00000433006.1:n.*110-219C>T
ENST00000485042.1:n.150C>T
NM_000380.3:c.674-219C>T , LRG_471t1:c.674-219C>T	NP_000371.1:n.674-219C>T
NR_027302.1:n.1022-219C>T
XM_006717278.1:c.674-219C>T	XP_006717341.1:n.674-219C>T
XM_011518988.1:c.674-219C>T	XP_011517290.1:n.674-219C>T
XR_929839.1:n.1169C>T
NM_001354975.1:c.548-219C>T	NP_001341904.1:n.548-219C>T
NR_149091.1:n.519-219C>T
NR_149092.1:n.685-219C>T
NR_149093.1:n.1175C>T
NR_149094.1:n.1069C>T
NM_000380.4:c.674-219C>T MANE Select	NP_000371.1:n.674-219C>T
NM_001354975.2:c.548-219C>T	NP_001341904.1:n.548-219C>T
NR_027302.2:n.953-219C>T
NR_149091.2:n.450-219C>T
NR_149092.2:n.616-219C>T
NR_149093.2:n.1106C>T
NR_149094.2:n.1000C>T