Canonical Allele Identifier: CA2340119
Gene: POMGNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43081189G>C , CM000665.2:g.43081189G>C GRCh38
NC_000003.11:g.43122681G>C , CM000665.1:g.43122681G>C GRCh37
NC_000003.10:g.43097685G>C NCBI36
NG_032930.1:g.29895C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032806.6:c.243C>G MANE Select NP_116195.2:p.Phe81Leu
ENST00000344697.3:c.243C>G MANE Select ENSP00000344125.2:p.Phe81Leu
NM_032806.5:c.243C>G NP_116195.2:p.Phe81Leu
ENST00000344697.2:c.243C>G ENSP00000344125.2:p.Phe81Leu
ENST00000441964.1:c.243C>G ENSP00000408992.1:p.Phe81Leu
ENST00000686643.1:c.243C>G ENSP00000509123.1:p.Phe81Leu
ENST00000687440.1:c.243C>G ENSP00000509610.1:p.Phe81Leu
ENST00000689987.1:c.243C>G ENSP00000510646.1:p.Phe81Leu
ENST00000690520.1:n.4188C>G
ENST00000692017.1:c.243C>G ENSP00000510571.1:p.Phe81Leu
ENST00000693717.1:c.243C>G ENSP00000510801.1:p.Phe81Leu
XM_005265515.1:c.243C>G XP_005265572.1:p.Phe81Leu
XM_005265515.3:c.243C>G XP_005265572.1:p.Phe81Leu
XM_011534163.1:c.243C>G XP_011532465.1:p.Phe81Leu
XM_011534163.2:c.243C>G XP_011532465.1:p.Phe81Leu
XM_011534164.1:c.243C>G XP_011532466.1:p.Phe81Leu
XM_017007353.1:c.243C>G XP_016862842.1:p.Phe81Leu