Canonical Allele Identifier: CA2690901643
Gene: XPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97675356_97675361dup , CM000671.2:g.97675356_97675361dup GRCh38
NC_000009.11:g.100437638_100437643dup , CM000671.1:g.100437638_100437643dup GRCh37
NC_000009.10:g.99477459_99477464dup NCBI36
NG_011642.1:g.27053_27058dup , LRG_471:g.27053_27058dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375128.5:c.*82_*87dup MANE Select ENSP00000364270.5:n.*82_*87dup
ENST00000375128.4:c.*82_*87dup ENSP00000364270.4:n.*82_*87dup
ENST00000462523.5:c.*340_*345dup ENSP00000433006.1:n.*340_*345dup
ENST00000485042.1:n.416_421dup
NM_000380.3:c.*82_*87dup , LRG_471t1:c.*82_*87dup NP_000371.1:n.*82_*87dup
NR_027302.1:n.1252_1257dup
XM_006717278.1:c.772+132_772+137dup XP_006717341.1:n.772+132_772+137dup
XM_011518988.1:c.772+132_772+137dup XP_011517290.1:n.772+132_772+137dup
NM_001354975.1:c.*82_*87dup NP_001341904.1:n.*82_*87dup
NR_149091.1:n.749_754dup
NR_149092.1:n.915_920dup
NR_149093.1:n.1441_1446dup
NR_149094.1:n.1335_1340dup
NM_000380.4:c.*82_*87dup MANE Select NP_000371.1:n.*82_*87dup
NM_001354975.2:c.*82_*87dup NP_001341904.1:n.*82_*87dup
NR_027302.2:n.1183_1188dup
NR_149091.2:n.680_685dup
NR_149092.2:n.846_851dup
NR_149093.2:n.1372_1377dup
NR_149094.2:n.1266_1271dup