Canonical Allele Identifier: CA868996352

Gene: XPA

Linked Data

• dbSNP Id: rs1350728392
• gnomAD v4: 9-97675799-G-A
• MyVariant Identifiers: chr9:g.100438081G>A (hg19) ; chr9:g.97675799G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675799G>A , CM000671.2:g.97675799G>A	GRCh38
NC_000009.11:g.100438081G>A , CM000671.1:g.100438081G>A	GRCh37
NC_000009.10:g.99477902G>A	NCBI36
NG_011642.1:g.26611C>T , LRG_471:g.26611C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-212C>T MANE Select	ENSP00000364270.5:n.674-212C>T
ENST00000375128.4:c.674-212C>T	ENSP00000364270.4:n.674-212C>T
ENST00000462523.5:c.*110-212C>T	ENSP00000433006.1:n.*110-212C>T
ENST00000485042.1:n.157C>T
NM_000380.3:c.674-212C>T , LRG_471t1:c.674-212C>T	NP_000371.1:n.674-212C>T
NR_027302.1:n.1022-212C>T
XM_006717278.1:c.674-212C>T	XP_006717341.1:n.674-212C>T
XM_011518988.1:c.674-212C>T	XP_011517290.1:n.674-212C>T
XR_929839.1:n.1176C>T
NM_001354975.1:c.548-212C>T	NP_001341904.1:n.548-212C>T
NR_149091.1:n.519-212C>T
NR_149092.1:n.685-212C>T
NR_149093.1:n.1182C>T
NR_149094.1:n.1076C>T
NM_000380.4:c.674-212C>T MANE Select	NP_000371.1:n.674-212C>T
NM_001354975.2:c.548-212C>T	NP_001341904.1:n.548-212C>T
NR_027302.2:n.953-212C>T
NR_149091.2:n.450-212C>T
NR_149092.2:n.616-212C>T
NR_149093.2:n.1113C>T
NR_149094.2:n.1007C>T