Canonical Allele Identifier: CA2579395764

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675682_97675687del , CM000671.2:g.97675682_97675687del	GRCh38
NC_000009.11:g.100437964_100437969del , CM000671.1:g.100437964_100437969del	GRCh37
NC_000009.10:g.99477785_99477790del	NCBI36
NG_011642.1:g.26728_26733del , LRG_471:g.26728_26733del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-95_674-90del MANE Select	ENSP00000364270.5:n.674-95_674-90del
ENST00000375128.4:c.674-95_674-90del	ENSP00000364270.4:n.674-95_674-90del
ENST00000462523.5:c.*110-95_*110-90del	ENSP00000433006.1:n.*110-95_*110-90del
ENST00000485042.1:n.185+89_186-90del
NM_000380.3:c.674-95_674-90del , LRG_471t1:c.674-95_674-90del	NP_000371.1:n.674-95_674-90del
NR_027302.1:n.1022-95_1022-90del
XM_006717278.1:c.674-95_674-90del	XP_006717341.1:n.674-95_674-90del
XM_011518988.1:c.674-95_674-90del	XP_011517290.1:n.674-95_674-90del
XR_929839.1:n.1204+89_1205-90del
NM_001354975.1:c.548-95_548-90del	NP_001341904.1:n.548-95_548-90del
NR_149091.1:n.519-95_519-90del
NR_149092.1:n.685-95_685-90del
NR_149093.1:n.1210+89_1211-90del
NR_149094.1:n.1104+89_1105-90del
NM_000380.4:c.674-95_674-90del MANE Select	NP_000371.1:n.674-95_674-90del
NM_001354975.2:c.548-95_548-90del	NP_001341904.1:n.548-95_548-90del
NR_027302.2:n.953-95_953-90del
NR_149091.2:n.450-95_450-90del
NR_149092.2:n.616-95_616-90del
NR_149093.2:n.1141+89_1142-90del
NR_149094.2:n.1035+89_1036-90del