Canonical Allele Identifier: CA2690901785

Gene: XPA

Linked Data

• gnomAD v4: 9-97675776-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675776T>A , CM000671.2:g.97675776T>A	GRCh38
NC_000009.11:g.100438058T>A , CM000671.1:g.100438058T>A	GRCh37
NC_000009.10:g.99477879T>A	NCBI36
NG_011642.1:g.26634A>T , LRG_471:g.26634A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-189A>T MANE Select	ENSP00000364270.5:n.674-189A>T
ENST00000375128.4:c.674-189A>T	ENSP00000364270.4:n.674-189A>T
ENST00000462523.5:c.*110-189A>T	ENSP00000433006.1:n.*110-189A>T
ENST00000485042.1:n.180A>T
NM_000380.3:c.674-189A>T , LRG_471t1:c.674-189A>T	NP_000371.1:n.674-189A>T
NR_027302.1:n.1022-189A>T
XM_006717278.1:c.674-189A>T	XP_006717341.1:n.674-189A>T
XM_011518988.1:c.674-189A>T	XP_011517290.1:n.674-189A>T
XR_929839.1:n.1199A>T
NM_001354975.1:c.548-189A>T	NP_001341904.1:n.548-189A>T
NR_149091.1:n.519-189A>T
NR_149092.1:n.685-189A>T
NR_149093.1:n.1205A>T
NR_149094.1:n.1099A>T
NM_000380.4:c.674-189A>T MANE Select	NP_000371.1:n.674-189A>T
NM_001354975.2:c.548-189A>T	NP_001341904.1:n.548-189A>T
NR_027302.2:n.953-189A>T
NR_149091.2:n.450-189A>T
NR_149092.2:n.616-189A>T
NR_149093.2:n.1136A>T
NR_149094.2:n.1030A>T