Canonical Allele Identifier: CA343843159

Gene: XPR1

Linked Data

• MyVariant Identifiers: chr1:g.180772655C>G (hg19) ; chr1:g.180803519C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180803519C>G , CM000663.2:g.180803519C>G	GRCh38
NC_000001.10:g.180772655C>G , CM000663.1:g.180772655C>G	GRCh37
NC_000001.9:g.179039278C>G	NCBI36
NG_050964.1:g.176510C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367590.9:c.355C>G MANE Select	ENSP00000356562.4:p.His119Asp
ENST00000367589.3:c.355C>G	ENSP00000356561.3:p.His119Asp
ENST00000367590.8:c.355C>G	ENSP00000356562.4:p.His119Asp
NM_001135669.1:c.355C>G	NP_001129141.1:p.His119Asp
NM_004736.3:c.355C>G	NP_004727.2:p.His119Asp
NM_001328662.1:c.355C>G	NP_001315591.1:p.His119Asp
NR_137330.1:n.547C>G
NM_001135669.2:c.355C>G	NP_001129141.1:p.His119Asp
NM_001328662.2:c.355C>G	NP_001315591.1:p.His119Asp
NM_004736.4:c.355C>G MANE Select	NP_004727.2:p.His119Asp
NR_137330.2:n.535C>G