Canonical Allele Identifier: CA1866632407

Gene: XPA

Linked Data

• dbSNP Id: rs1828343830
• gnomAD v4: 9-97675716-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675718dup , CM000671.2:g.97675718dup	GRCh38
NC_000009.11:g.100438000dup , CM000671.1:g.100438000dup	GRCh37
NC_000009.10:g.99477821dup	NCBI36
NG_011642.1:g.26693dup , LRG_471:g.26693dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-130dup MANE Select	ENSP00000364270.5:n.674-130dup
ENST00000375128.4:c.674-130dup	ENSP00000364270.4:n.674-130dup
ENST00000462523.5:c.*110-130dup	ENSP00000433006.1:n.*110-130dup
ENST00000485042.1:n.185+54dup
NM_000380.3:c.674-130dup , LRG_471t1:c.674-130dup	NP_000371.1:n.674-130dup
NR_027302.1:n.1022-130dup
XM_006717278.1:c.674-130dup	XP_006717341.1:n.674-130dup
XM_011518988.1:c.674-130dup	XP_011517290.1:n.674-130dup
XR_929839.1:n.1204+54dup
NM_001354975.1:c.548-130dup	NP_001341904.1:n.548-130dup
NR_149091.1:n.519-130dup
NR_149092.1:n.685-130dup
NR_149093.1:n.1210+54dup
NR_149094.1:n.1104+54dup
NM_000380.4:c.674-130dup MANE Select	NP_000371.1:n.674-130dup
NM_001354975.2:c.548-130dup	NP_001341904.1:n.548-130dup
NR_027302.2:n.953-130dup
NR_149091.2:n.450-130dup
NR_149092.2:n.616-130dup
NR_149093.2:n.1141+54dup
NR_149094.2:n.1035+54dup