Canonical Allele Identifier: CA422226287
Gene: XPR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.180772720C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803584C>T , CM000663.2:g.180803584C>T GRCh38
NC_000001.10:g.180772720C>T , CM000663.1:g.180772720C>T GRCh37
NC_000001.9:g.179039343C>T NCBI36
NG_050964.1:g.176575C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.420C>T MANE Select ENSP00000356562.4:p.Leu140=
ENST00000367589.3:c.420C>T ENSP00000356561.3:p.Leu140=
ENST00000367590.8:c.420C>T ENSP00000356562.4:p.Leu140=
NM_001135669.1:c.420C>T NP_001129141.1:p.Leu140=
NM_004736.3:c.420C>T NP_004727.2:p.Leu140=
NM_001328662.1:c.420C>T NP_001315591.1:p.Leu140=
NR_137330.1:n.612C>T
NM_001135669.2:c.420C>T NP_001129141.1:p.Leu140=
NM_001328662.2:c.420C>T NP_001315591.1:p.Leu140=
NM_004736.4:c.420C>T MANE Select NP_004727.2:p.Leu140=
NR_137330.2:n.600C>T