Canonical Allele Identifier: CA2690901757
Gene: XPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97675742_97675748del , CM000671.2:g.97675742_97675748del GRCh38
NC_000009.11:g.100438024_100438030del , CM000671.1:g.100438024_100438030del GRCh37
NC_000009.10:g.99477845_99477851del NCBI36
NG_011642.1:g.26662_26668del , LRG_471:g.26662_26668del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375128.5:c.674-161_674-155del MANE Select ENSP00000364270.5:n.674-161_674-155del
ENST00000375128.4:c.674-161_674-155del ENSP00000364270.4:n.674-161_674-155del
ENST00000462523.5:c.*110-161_*110-155del ENSP00000433006.1:n.*110-161_*110-155del
ENST00000485042.1:n.185+23_185+29del
NM_000380.3:c.674-161_674-155del , LRG_471t1:c.674-161_674-155del NP_000371.1:n.674-161_674-155del
NR_027302.1:n.1022-161_1022-155del
XM_006717278.1:c.674-161_674-155del XP_006717341.1:n.674-161_674-155del
XM_011518988.1:c.674-161_674-155del XP_011517290.1:n.674-161_674-155del
XR_929839.1:n.1204+23_1204+29del
NM_001354975.1:c.548-161_548-155del NP_001341904.1:n.548-161_548-155del
NR_149091.1:n.519-161_519-155del
NR_149092.1:n.685-161_685-155del
NR_149093.1:n.1210+23_1210+29del
NR_149094.1:n.1104+23_1104+29del
NM_000380.4:c.674-161_674-155del MANE Select NP_000371.1:n.674-161_674-155del
NM_001354975.2:c.548-161_548-155del NP_001341904.1:n.548-161_548-155del
NR_027302.2:n.953-161_953-155del
NR_149091.2:n.450-161_450-155del
NR_149092.2:n.616-161_616-155del
NR_149093.2:n.1141+23_1141+29del
NR_149094.2:n.1035+23_1035+29del