Canonical Allele Identifier: CA2340085

Gene: POMGNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43081010C>T , CM000665.2:g.43081010C>T	GRCh38
NC_000003.11:g.43122502C>T , CM000665.1:g.43122502C>T	GRCh37
NC_000003.10:g.43097506C>T	NCBI36
NG_032930.1:g.30074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686643.1:c.422G>A	ENSP00000509123.1:p.Arg141His
ENST00000687440.1:c.422G>A	ENSP00000509610.1:p.Arg141His
ENST00000689987.1:c.422G>A	ENSP00000510646.1:p.Arg141His
ENST00000690520.1:n.4367G>A
ENST00000692017.1:c.422G>A	ENSP00000510571.1:p.Arg141His
ENST00000693717.1:c.422G>A	ENSP00000510801.1:p.Arg141His
ENST00000344697.3:c.422G>A MANE Select	ENSP00000344125.2:p.Arg141His
ENST00000344697.2:c.422G>A	ENSP00000344125.2:p.Arg141His
ENST00000441964.1:c.422G>A	ENSP00000408992.1:p.Arg141His
NM_032806.5:c.422G>A	NP_116195.2:p.Arg141His
XM_005265515.1:c.422G>A	XP_005265572.1:p.Arg141His
XM_011534163.1:c.422G>A	XP_011532465.1:p.Arg141His
XM_011534164.1:c.422G>A	XP_011532466.1:p.Arg141His
XM_005265515.3:c.422G>A	XP_005265572.1:p.Arg141His
XM_011534163.2:c.422G>A	XP_011532465.1:p.Arg141His
XM_017007353.1:c.422G>A	XP_016862842.1:p.Arg141His
NM_032806.6:c.422G>A MANE Select	NP_116195.2:p.Arg141His