Canonical Allele Identifier: CA2339925

Gene: POMGNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43080309T>C , CM000665.2:g.43080309T>C	GRCh38
NC_000003.11:g.43121801T>C , CM000665.1:g.43121801T>C	GRCh37
NC_000003.10:g.43096805T>C	NCBI36
NG_032930.1:g.30775A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032806.6:c.1123A>G MANE Select	NP_116195.2:p.Thr375Ala
ENST00000344697.3:c.1123A>G MANE Select	ENSP00000344125.2:p.Thr375Ala
NM_032806.5:c.1123A>G	NP_116195.2:p.Thr375Ala
ENST00000344697.2:c.1123A>G	ENSP00000344125.2:p.Thr375Ala
ENST00000441964.1:c.1123A>G	ENSP00000408992.1:p.Thr375Ala
ENST00000686643.1:c.1123A>G	ENSP00000509123.1:p.Thr375Ala
ENST00000687440.1:c.1123A>G	ENSP00000509610.1:p.Thr375Ala
ENST00000689987.1:c.1123A>G	ENSP00000510646.1:p.Thr375Ala
ENST00000690520.1:n.5068A>G
ENST00000692017.1:c.1123A>G	ENSP00000510571.1:p.Thr375Ala
ENST00000693717.1:c.1123A>G	ENSP00000510801.1:p.Thr375Ala
XM_005265515.1:c.1123A>G	XP_005265572.1:p.Thr375Ala
XM_005265515.3:c.1123A>G	XP_005265572.1:p.Thr375Ala
XM_011534163.1:c.1123A>G	XP_011532465.1:p.Thr375Ala
XM_011534163.2:c.1123A>G	XP_011532465.1:p.Thr375Ala
XM_011534164.1:c.1123A>G	XP_011532466.1:p.Thr375Ala
XM_017007353.1:c.1123A>G	XP_016862842.1:p.Thr375Ala