Canonical Allele Identifier: CA2690901811

Gene: XPA

Linked Data

• gnomAD v4: 9-97675810-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675811del , CM000671.2:g.97675811del	GRCh38
NC_000009.11:g.100438093del , CM000671.1:g.100438093del	GRCh37
NC_000009.10:g.99477914del	NCBI36
NG_011642.1:g.26599del , LRG_471:g.26599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-224del MANE Select	ENSP00000364270.5:n.674-224del
ENST00000375128.4:c.674-224del	ENSP00000364270.4:n.674-224del
ENST00000462523.5:c.*110-224del	ENSP00000433006.1:n.*110-224del
ENST00000485042.1:n.145del
NM_000380.3:c.674-224del , LRG_471t1:c.674-224del	NP_000371.1:n.674-224del
NR_027302.1:n.1022-224del
XM_006717278.1:c.674-224del	XP_006717341.1:n.674-224del
XM_011518988.1:c.674-224del	XP_011517290.1:n.674-224del
XR_929839.1:n.1164del
NM_001354975.1:c.548-224del	NP_001341904.1:n.548-224del
NR_149091.1:n.519-224del
NR_149092.1:n.685-224del
NR_149093.1:n.1170del
NR_149094.1:n.1064del
NM_000380.4:c.674-224del MANE Select	NP_000371.1:n.674-224del
NM_001354975.2:c.548-224del	NP_001341904.1:n.548-224del
NR_027302.2:n.953-224del
NR_149091.2:n.450-224del
NR_149092.2:n.616-224del
NR_149093.2:n.1101del
NR_149094.2:n.995del