Canonical Allele Identifier: CA422226216
Gene: XPR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.180772612T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803476T>A , CM000663.2:g.180803476T>A GRCh38
NC_000001.10:g.180772612T>A , CM000663.1:g.180772612T>A GRCh37
NC_000001.9:g.179039235T>A NCBI36
NG_050964.1:g.176467T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.312T>A MANE Select ENSP00000356562.4:p.Val104=
ENST00000367589.3:c.312T>A ENSP00000356561.3:p.Val104=
ENST00000367590.8:c.312T>A ENSP00000356562.4:p.Val104=
NM_001135669.1:c.312T>A NP_001129141.1:p.Val104=
NM_004736.3:c.312T>A NP_004727.2:p.Val104=
NM_001328662.1:c.312T>A NP_001315591.1:p.Val104=
NR_137330.1:n.504T>A
NM_001135669.2:c.312T>A NP_001129141.1:p.Val104=
NM_001328662.2:c.312T>A NP_001315591.1:p.Val104=
NM_004736.4:c.312T>A MANE Select NP_004727.2:p.Val104=
NR_137330.2:n.492T>A