Canonical Allele Identifier: CA343842935
Gene: XPR1 HGNC NCBI

Linked Data

dbSNP Id: rs1374007102

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803413G>T , CM000663.2:g.180803413G>T GRCh38
NC_000001.10:g.180772549G>T , CM000663.1:g.180772549G>T GRCh37
NC_000001.9:g.179039172G>T NCBI36
NG_050964.1:g.176404G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.249G>T MANE Select ENSP00000356562.4:p.Arg83Ser
ENST00000367589.3:c.249G>T ENSP00000356561.3:p.Arg83Ser
ENST00000367590.8:c.249G>T ENSP00000356562.4:p.Arg83Ser
NM_001135669.1:c.249G>T NP_001129141.1:p.Arg83Ser
NM_004736.3:c.249G>T NP_004727.2:p.Arg83Ser
NM_001328662.1:c.249G>T NP_001315591.1:p.Arg83Ser
NR_137330.1:n.441G>T
NM_001135669.2:c.249G>T NP_001129141.1:p.Arg83Ser
NM_001328662.2:c.249G>T NP_001315591.1:p.Arg83Ser
NM_004736.4:c.249G>T MANE Select NP_004727.2:p.Arg83Ser
NR_137330.2:n.429G>T