Canonical Allele Identifier: CA400428934

Gene: PTRH2

Linked Data

• MyVariant Identifiers: chr17:g.57774930C>T (hg19) ; chr17:g.59697569C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59697569C>T , CM000679.2:g.59697569C>T	GRCh38
NC_000017.10:g.57774930C>T , CM000679.1:g.57774930C>T	GRCh37
NC_000017.9:g.55129712C>T	NCBI36
NG_042064.1:g.15030G>A
NG_047043.1:g.82881C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393038.3:c.410G>A MANE Select	ENSP00000376758.2:p.Gly137Glu
ENST00000393038.2:c.410G>A	ENSP00000376758.2:p.Gly137Glu
ENST00000409433.2:c.413G>A	ENSP00000387180.2:p.Gly138Glu
ENST00000470557.2:c.410G>A	ENSP00000464327.1:p.Gly137Glu
ENST00000587935.1:n.45+9802G>A
NM_001015509.2:c.413G>A	NP_001015509.1:p.Gly138Glu
NM_016077.3:c.410G>A	NP_057161.1:p.Gly137Glu
NM_016077.4:c.410G>A	NP_057161.1:p.Gly137Glu
XM_011524887.1:c.410G>A	XP_011523189.1:p.Gly137Glu
XM_011524887.2:c.410G>A	XP_011523189.1:p.Gly137Glu
NM_016077.5:c.410G>A MANE Select	NP_057161.1:p.Gly137Glu
NM_001015509.3:c.413G>A	NP_001015509.1:p.Gly138Glu