Canonical Allele Identifier: CA374188116
Community Standard Title: NM_000380.4(XPA):c.235G>T (p.Glu79Ter)
Gene: XPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97693697C>A , CM000671.2:g.97693697C>A GRCh38
NC_000009.11:g.100455979C>A , CM000671.1:g.100455979C>A GRCh37
NC_000009.10:g.99495800C>A NCBI36
NG_011642.1:g.8713G>T , LRG_471:g.8713G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000380.4:c.235G>T MANE Select NP_000371.1:p.Glu79Ter
ENST00000375128.5:c.235G>T MANE Select ENSP00000364270.5:p.Glu79Ter
NM_000380.3:c.235G>T , LRG_471t1:c.235G>T NP_000371.1:p.Glu79Ter
NM_001354975.1:c.109G>T NP_001341904.1:p.Glu37Ter
NM_001354975.2:c.109G>T NP_001341904.1:p.Glu37Ter
NR_027302.1:n.352G>T
NR_027302.2:n.283G>T
NR_149091.1:n.352G>T
NR_149091.2:n.283G>T
NR_149092.1:n.352G>T
NR_149092.2:n.283G>T
NR_149093.1:n.352G>T
NR_149093.2:n.283G>T
NR_149094.1:n.352G>T
NR_149094.2:n.283G>T
ENST00000375128.4:c.235G>T ENSP00000364270.4:p.Glu79Ter
ENST00000462523.5:c.235G>T ENSP00000433006.1:p.Glu79Ter
ENST00000496104.1:n.135G>T
XM_006717278.1:c.235G>T XP_006717341.1:p.Glu79Ter
XM_011518988.1:c.235G>T XP_011517290.1:p.Glu79Ter
XR_929839.1:n.346G>T