Canonical Allele Identifier: CA2690901735

Gene: XPA

Linked Data

• gnomAD v4: 9-97675705-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675705A>G , CM000671.2:g.97675705A>G	GRCh38
NC_000009.11:g.100437987A>G , CM000671.1:g.100437987A>G	GRCh37
NC_000009.10:g.99477808A>G	NCBI36
NG_011642.1:g.26705T>C , LRG_471:g.26705T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-118T>C MANE Select	ENSP00000364270.5:n.674-118T>C
ENST00000375128.4:c.674-118T>C	ENSP00000364270.4:n.674-118T>C
ENST00000462523.5:c.*110-118T>C	ENSP00000433006.1:n.*110-118T>C
ENST00000485042.1:n.185+66T>C
NM_000380.3:c.674-118T>C , LRG_471t1:c.674-118T>C	NP_000371.1:n.674-118T>C
NR_027302.1:n.1022-118T>C
XM_006717278.1:c.674-118T>C	XP_006717341.1:n.674-118T>C
XM_011518988.1:c.674-118T>C	XP_011517290.1:n.674-118T>C
XR_929839.1:n.1204+66T>C
NM_001354975.1:c.548-118T>C	NP_001341904.1:n.548-118T>C
NR_149091.1:n.519-118T>C
NR_149092.1:n.685-118T>C
NR_149093.1:n.1210+66T>C
NR_149094.1:n.1104+66T>C
NM_000380.4:c.674-118T>C MANE Select	NP_000371.1:n.674-118T>C
NM_001354975.2:c.548-118T>C	NP_001341904.1:n.548-118T>C
NR_027302.2:n.953-118T>C
NR_149091.2:n.450-118T>C
NR_149092.2:n.616-118T>C
NR_149093.2:n.1141+66T>C
NR_149094.2:n.1035+66T>C