Canonical Allele Identifier: CA1866632421

Gene: XPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97675754_97675756delinsCAA , CM000671.2:g.97675754_97675756delinsCAA	GRCh38
NC_000009.11:g.100438036_100438038delinsCAA , CM000671.1:g.100438036_100438038delinsCAA	GRCh37
NC_000009.10:g.99477857_99477859delinsCAA	NCBI36
NG_011642.1:g.26654_26656delinsTTG , LRG_471:g.26654_26656delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375128.5:c.674-169_674-167delinsTTG MANE Select	ENSP00000364270.5:n.674-169_674-167delinsTTG
ENST00000375128.4:c.674-169_674-167delinsTTG	ENSP00000364270.4:n.674-169_674-167delinsTTG
ENST00000462523.5:c.*110-169_*110-167delinsTTG	ENSP00000433006.1:n.*110-169_*110-167delinsTTG
ENST00000485042.1:n.185+15_185+17delinsTTG
NM_000380.3:c.674-169_674-167delinsTTG , LRG_471t1:c.674-169_674-167delinsTTG	NP_000371.1:n.674-169_674-167delinsTTG
NR_027302.1:n.1022-169_1022-167delinsTTG
XM_006717278.1:c.674-169_674-167delinsTTG	XP_006717341.1:n.674-169_674-167delinsTTG
XM_011518988.1:c.674-169_674-167delinsTTG	XP_011517290.1:n.674-169_674-167delinsTTG
XR_929839.1:n.1204+15_1204+17delinsTTG
NM_001354975.1:c.548-169_548-167delinsTTG	NP_001341904.1:n.548-169_548-167delinsTTG
NR_149091.1:n.519-169_519-167delinsTTG
NR_149092.1:n.685-169_685-167delinsTTG
NR_149093.1:n.1210+15_1210+17delinsTTG
NR_149094.1:n.1104+15_1104+17delinsTTG
NM_000380.4:c.674-169_674-167delinsTTG MANE Select	NP_000371.1:n.674-169_674-167delinsTTG
NM_001354975.2:c.548-169_548-167delinsTTG	NP_001341904.1:n.548-169_548-167delinsTTG
NR_027302.2:n.953-169_953-167delinsTTG
NR_149091.2:n.450-169_450-167delinsTTG
NR_149092.2:n.616-169_616-167delinsTTG
NR_149093.2:n.1141+15_1141+17delinsTTG
NR_149094.2:n.1035+15_1035+17delinsTTG