Canonical Allele Identifier: CA1210833195
Gene: XPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803598T= , CM000663.2:g.180803598T= GRCh38
NC_000001.10:g.180772734T= , CM000663.1:g.180772734T= GRCh37
NC_000001.9:g.179039357T= NCBI36
NG_050964.1:g.176589T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.434T= MANE Select ENSP00000356562.4:p.Leu145=
ENST00000367589.3:c.434T= ENSP00000356561.3:p.Leu145=
ENST00000367590.8:c.434T= ENSP00000356562.4:p.Leu145=
NM_001135669.1:c.434T= NP_001129141.1:p.Leu145=
NM_004736.3:c.434T= NP_004727.2:p.Leu145=
NM_001328662.1:c.434T= NP_001315591.1:p.Leu145=
NR_137330.1:n.626T=
NM_001135669.2:c.434T= NP_001129141.1:p.Leu145=
NM_001328662.2:c.434T= NP_001315591.1:p.Leu145=
NM_004736.4:c.434T= MANE Select NP_004727.2:p.Leu145=
NR_137330.2:n.614T=