Canonical Allele Identifier: CA2690901803

Gene: XPA

Linked Data

• gnomAD v4: 9-97675803-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675803C>A , CM000671.2:g.97675803C>A	GRCh38
NC_000009.11:g.100438085C>A , CM000671.1:g.100438085C>A	GRCh37
NC_000009.10:g.99477906C>A	NCBI36
NG_011642.1:g.26607G>T , LRG_471:g.26607G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-216G>T MANE Select	ENSP00000364270.5:n.674-216G>T
ENST00000375128.4:c.674-216G>T	ENSP00000364270.4:n.674-216G>T
ENST00000462523.5:c.*110-216G>T	ENSP00000433006.1:n.*110-216G>T
ENST00000485042.1:n.153G>T
NM_000380.3:c.674-216G>T , LRG_471t1:c.674-216G>T	NP_000371.1:n.674-216G>T
NR_027302.1:n.1022-216G>T
XM_006717278.1:c.674-216G>T	XP_006717341.1:n.674-216G>T
XM_011518988.1:c.674-216G>T	XP_011517290.1:n.674-216G>T
XR_929839.1:n.1172G>T
NM_001354975.1:c.548-216G>T	NP_001341904.1:n.548-216G>T
NR_149091.1:n.519-216G>T
NR_149092.1:n.685-216G>T
NR_149093.1:n.1178G>T
NR_149094.1:n.1072G>T
NM_000380.4:c.674-216G>T MANE Select	NP_000371.1:n.674-216G>T
NM_001354975.2:c.548-216G>T	NP_001341904.1:n.548-216G>T
NR_027302.2:n.953-216G>T
NR_149091.2:n.450-216G>T
NR_149092.2:n.616-216G>T
NR_149093.2:n.1109G>T
NR_149094.2:n.1003G>T