Canonical Allele Identifier: CA2690901828

Gene: XPA

Linked Data

• gnomAD v4: 9-97675843-GGGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675847_97675850del , CM000671.2:g.97675847_97675850del	GRCh38
NC_000009.11:g.100438129_100438132del , CM000671.1:g.100438129_100438132del	GRCh37
NC_000009.10:g.99477950_99477953del	NCBI36
NG_011642.1:g.26563_26566del , LRG_471:g.26563_26566del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-260_674-257del MANE Select	ENSP00000364270.5:n.674-260_674-257del
ENST00000375128.4:c.674-260_674-257del	ENSP00000364270.4:n.674-260_674-257del
ENST00000462523.5:c.*110-260_*110-257del	ENSP00000433006.1:n.*110-260_*110-257del
ENST00000485042.1:n.109_112del
NM_000380.3:c.674-260_674-257del , LRG_471t1:c.674-260_674-257del	NP_000371.1:n.674-260_674-257del
NR_027302.1:n.1022-260_1022-257del
XM_006717278.1:c.674-260_674-257del	XP_006717341.1:n.674-260_674-257del
XM_011518988.1:c.674-260_674-257del	XP_011517290.1:n.674-260_674-257del
XR_929839.1:n.1128_1131del
NM_001354975.1:c.548-260_548-257del	NP_001341904.1:n.548-260_548-257del
NR_149091.1:n.519-260_519-257del
NR_149092.1:n.685-260_685-257del
NR_149093.1:n.1134_1137del
NR_149094.1:n.1028_1031del
NM_000380.4:c.674-260_674-257del MANE Select	NP_000371.1:n.674-260_674-257del
NM_001354975.2:c.548-260_548-257del	NP_001341904.1:n.548-260_548-257del
NR_027302.2:n.953-260_953-257del
NR_149091.2:n.450-260_450-257del
NR_149092.2:n.616-260_616-257del
NR_149093.2:n.1065_1068del
NR_149094.2:n.959_962del