Canonical Allele Identifier: CA1866632302
Gene: XPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97675570T= , CM000671.2:g.97675570T= GRCh38
NC_000009.11:g.100437852T= , CM000671.1:g.100437852T= GRCh37
NC_000009.10:g.99477673T= NCBI36
NG_011642.1:g.26840A= , LRG_471:g.26840A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375128.5:c.691A= MANE Select ENSP00000364270.5:p.Arg231=
ENST00000375128.4:c.691A= ENSP00000364270.4:p.Arg231=
ENST00000462523.5:c.*127A= ENSP00000433006.1:n.*127A=
ENST00000485042.1:n.203A=
NM_000380.3:c.691A= , LRG_471t1:c.691A= NP_000371.1:p.Arg231=
NR_027302.1:n.1039A=
XM_006717278.1:c.691A= XP_006717341.1:p.Arg231=
XM_011518988.1:c.691A= XP_011517290.1:p.Arg231=
XR_929839.1:n.1222A=
NM_001354975.1:c.565A= NP_001341904.1:p.Arg189=
NR_149091.1:n.536A=
NR_149092.1:n.702A=
NR_149093.1:n.1228A=
NR_149094.1:n.1122A=
NM_000380.4:c.691A= MANE Select NP_000371.1:p.Arg231=
NM_001354975.2:c.565A= NP_001341904.1:p.Arg189=
NR_027302.2:n.970A=
NR_149091.2:n.467A=
NR_149092.2:n.633A=
NR_149093.2:n.1159A=
NR_149094.2:n.1053A=