Canonical Allele Identifier: CA422226158
Gene: XPR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.180772531C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803395C>A , CM000663.2:g.180803395C>A GRCh38
NC_000001.10:g.180772531C>A , CM000663.1:g.180772531C>A GRCh37
NC_000001.9:g.179039154C>A NCBI36
NG_050964.1:g.176386C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.231C>A MANE Select ENSP00000356562.4:p.Leu77=
ENST00000367589.3:c.231C>A ENSP00000356561.3:p.Leu77=
ENST00000367590.8:c.231C>A ENSP00000356562.4:p.Leu77=
NM_001135669.1:c.231C>A NP_001129141.1:p.Leu77=
NM_004736.3:c.231C>A NP_004727.2:p.Leu77=
NM_001328662.1:c.231C>A NP_001315591.1:p.Leu77=
NR_137330.1:n.423C>A
NM_001135669.2:c.231C>A NP_001129141.1:p.Leu77=
NM_001328662.2:c.231C>A NP_001315591.1:p.Leu77=
NM_004736.4:c.231C>A MANE Select NP_004727.2:p.Leu77=
NR_137330.2:n.411C>A