Canonical Allele Identifier: CA2690901781

Gene: XPA

Linked Data

• gnomAD v4: 9-97675773-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675773C>A , CM000671.2:g.97675773C>A	GRCh38
NC_000009.11:g.100438055C>A , CM000671.1:g.100438055C>A	GRCh37
NC_000009.10:g.99477876C>A	NCBI36
NG_011642.1:g.26637G>T , LRG_471:g.26637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-186G>T MANE Select	ENSP00000364270.5:n.674-186G>T
ENST00000375128.4:c.674-186G>T	ENSP00000364270.4:n.674-186G>T
ENST00000462523.5:c.*110-186G>T	ENSP00000433006.1:n.*110-186G>T
ENST00000485042.1:n.183G>T
NM_000380.3:c.674-186G>T , LRG_471t1:c.674-186G>T	NP_000371.1:n.674-186G>T
NR_027302.1:n.1022-186G>T
XM_006717278.1:c.674-186G>T	XP_006717341.1:n.674-186G>T
XM_011518988.1:c.674-186G>T	XP_011517290.1:n.674-186G>T
XR_929839.1:n.1202G>T
NM_001354975.1:c.548-186G>T	NP_001341904.1:n.548-186G>T
NR_149091.1:n.519-186G>T
NR_149092.1:n.685-186G>T
NR_149093.1:n.1208G>T
NR_149094.1:n.1102G>T
NM_000380.4:c.674-186G>T MANE Select	NP_000371.1:n.674-186G>T
NM_001354975.2:c.548-186G>T	NP_001341904.1:n.548-186G>T
NR_027302.2:n.953-186G>T
NR_149091.2:n.450-186G>T
NR_149092.2:n.616-186G>T
NR_149093.2:n.1139G>T
NR_149094.2:n.1033G>T