Canonical Allele Identifier: CA5148953

Gene: XPA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97697296T>G , CM000671.2:g.97697296T>G	GRCh38
NC_000009.11:g.100459578T>G , CM000671.1:g.100459578T>G	GRCh37
NC_000009.10:g.99499399T>G	NCBI36
NG_011642.1:g.5114A>C , LRG_471:g.5114A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.-4A>C MANE Select	ENSP00000364270.5:n.-4A>C
ENST00000375128.4:c.-4A>C	ENSP00000364270.4:n.-4A>C
NM_000380.3:c.-4A>C , LRG_471t1:c.-4A>C	NP_000371.1:n.-4A>C
NR_027302.1:n.114A>C
XM_006717278.1:c.-4A>C	XP_006717341.1:n.-4A>C
XM_011518988.1:c.-4A>C	XP_011517290.1:n.-4A>C
XR_929839.1:n.108A>C
NM_001354975.1:c.-1153A>C	NP_001341904.1:n.-1153A>C
NR_149091.1:n.114A>C
NR_149092.1:n.114A>C
NR_149093.1:n.114A>C
NR_149094.1:n.114A>C
NM_000380.4:c.-4A>C MANE Select	NP_000371.1:n.-4A>C
NM_001354975.2:c.-1153A>C	NP_001341904.1:n.-1153A>C
NR_027302.2:n.45A>C
NR_149091.2:n.45A>C
NR_149092.2:n.45A>C
NR_149093.2:n.45A>C
NR_149094.2:n.45A>C