Canonical Allele Identifier: CA343842885
Gene: XPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180803391A>C , CM000663.2:g.180803391A>C GRCh38
NC_000001.10:g.180772527A>C , CM000663.1:g.180772527A>C GRCh37
NC_000001.9:g.179039150A>C NCBI36
NG_050964.1:g.176382A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367590.9:c.227A>C MANE Select ENSP00000356562.4:p.Lys76Thr
ENST00000367589.3:c.227A>C ENSP00000356561.3:p.Lys76Thr
ENST00000367590.8:c.227A>C ENSP00000356562.4:p.Lys76Thr
NM_001135669.1:c.227A>C NP_001129141.1:p.Lys76Thr
NM_004736.3:c.227A>C NP_004727.2:p.Lys76Thr
NM_001328662.1:c.227A>C NP_001315591.1:p.Lys76Thr
NR_137330.1:n.419A>C
NM_001135669.2:c.227A>C NP_001129141.1:p.Lys76Thr
NM_001328662.2:c.227A>C NP_001315591.1:p.Lys76Thr
NM_004736.4:c.227A>C MANE Select NP_004727.2:p.Lys76Thr
NR_137330.2:n.407A>C