Canonical Allele Identifier: CA422226227
Gene: XPR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.180772624A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803488A>C , CM000663.2:g.180803488A>C GRCh38
NC_000001.10:g.180772624A>C , CM000663.1:g.180772624A>C GRCh37
NC_000001.9:g.179039247A>C NCBI36
NG_050964.1:g.176479A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367590.9:c.324A>C MANE Select ENSP00000356562.4:p.Arg108=
ENST00000367589.3:c.324A>C ENSP00000356561.3:p.Arg108=
ENST00000367590.8:c.324A>C ENSP00000356562.4:p.Arg108=
NM_001135669.1:c.324A>C NP_001129141.1:p.Arg108=
NM_004736.3:c.324A>C NP_004727.2:p.Arg108=
NM_001328662.1:c.324A>C NP_001315591.1:p.Arg108=
NR_137330.1:n.516A>C
NM_001135669.2:c.324A>C NP_001129141.1:p.Arg108=
NM_001328662.2:c.324A>C NP_001315591.1:p.Arg108=
NM_004736.4:c.324A>C MANE Select NP_004727.2:p.Arg108=
NR_137330.2:n.504A>C