Canonical Allele Identifier: CA2690901677

Gene: XPA

Linked Data

• gnomAD v4: 9-97675395-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675395A>G , CM000671.2:g.97675395A>G	GRCh38
NC_000009.11:g.100437677A>G , CM000671.1:g.100437677A>G	GRCh37
NC_000009.10:g.99477498A>G	NCBI36
NG_011642.1:g.27015T>C , LRG_471:g.27015T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.*44T>C MANE Select	ENSP00000364270.5:n.*44T>C
ENST00000375128.4:c.*44T>C	ENSP00000364270.4:n.*44T>C
ENST00000462523.5:c.*302T>C	ENSP00000433006.1:n.*302T>C
ENST00000485042.1:n.378T>C
NM_000380.3:c.*44T>C , LRG_471t1:c.*44T>C	NP_000371.1:n.*44T>C
NR_027302.1:n.1214T>C
XM_006717278.1:c.772+94T>C	XP_006717341.1:n.772+94T>C
XM_011518988.1:c.772+94T>C	XP_011517290.1:n.772+94T>C
NM_001354975.1:c.*44T>C	NP_001341904.1:n.*44T>C
NR_149091.1:n.711T>C
NR_149092.1:n.877T>C
NR_149093.1:n.1403T>C
NR_149094.1:n.1297T>C
NM_000380.4:c.*44T>C MANE Select	NP_000371.1:n.*44T>C
NM_001354975.2:c.*44T>C	NP_001341904.1:n.*44T>C
NR_027302.2:n.1145T>C
NR_149091.2:n.642T>C
NR_149092.2:n.808T>C
NR_149093.2:n.1334T>C
NR_149094.2:n.1228T>C