Canonical Allele Identifier: CA7425934

Gene: NIPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22851830G>A , CM000677.2:g.22851830G>A	GRCh38
NC_000015.9:g.23021238C>T , CM000677.1:g.23021238C>T	GRCh37
NC_000015.8:g.20572679C>T	NCBI36
NG_021303.1:g.18190G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337451.8:c.99G>A MANE Select	ENSP00000337618.3:p.Lys33=
ENST00000398014.7:c.99G>A	ENSP00000381096.3:p.Lys33=
ENST00000674173.1:c.99G>A	ENSP00000501408.1:p.Lys33=
ENST00000674215.1:n.789G>A
ENST00000674289.1:c.99G>A	ENSP00000501412.1:p.Lys33=
ENST00000674330.1:c.99G>A	ENSP00000501373.1:p.Lys33=
ENST00000674477.1:c.99G>A	ENSP00000501489.1:p.Lys33=
ENST00000337451.7:c.99G>A	ENSP00000337618.3:p.Lys33=
ENST00000359727.8:c.99G>A	ENSP00000352762.4:p.Lys33=
ENST00000398013.7:c.99G>A	ENSP00000381095.3:p.Lys33=
ENST00000398014.6:c.99G>A	ENSP00000381096.2:p.Lys33=
ENST00000539711.2:c.99G>A	ENSP00000437746.2:p.Lys33=
ENST00000560039.1:c.99G>A	ENSP00000453700.1:p.Lys33=
NM_001008860.2:c.99G>A	NP_001008860.1:p.Lys33=
NM_001008892.2:c.99G>A	NP_001008892.1:p.Lys33=
NM_001008894.2:c.99G>A	NP_001008894.1:p.Lys33=
NM_001184888.1:c.99G>A	NP_001171817.1:p.Lys33=
NM_001184889.1:c.99G>A	NP_001171818.1:p.Lys33=
NM_030922.6:c.99G>A	NP_112184.4:p.Lys33=
XM_005272546.2:c.99G>A	XP_005272603.1:p.Lys33=
XM_005272547.3:c.99G>A	XP_005272604.1:p.Lys33=
XM_005272548.2:c.99G>A	XP_005272605.1:p.Lys33=
XM_005272549.2:c.99G>A	XP_005272606.1:p.Lys33=
XM_005272550.2:c.99G>A	XP_005272607.1:p.Lys33=
XM_005272552.2:c.99G>A	XP_005272609.1:p.Lys33=
XM_005272553.3:c.99G>A	XP_005272610.1:p.Lys33=
XM_006720364.1:c.99G>A	XP_006720427.1:p.Lys33=
XM_006720365.1:c.99G>A	XP_006720428.1:p.Lys33=
XM_006720366.2:c.99G>A	XP_006720429.1:p.Lys33=
XM_006720367.1:c.99G>A	XP_006720430.1:p.Lys33=
XM_011543877.1:c.99G>A	XP_011542179.1:p.Lys33=
XM_011543878.1:c.99G>A	XP_011542180.1:p.Lys33=
XM_011543879.1:c.99G>A	XP_011542181.1:p.Lys33=
XM_011543880.1:c.99G>A	XP_011542182.1:p.Lys33=
XM_011543881.1:c.99G>A	XP_011542183.1:p.Lys33=
XM_005272546.3:c.99G>A	XP_005272603.1:p.Lys33=
XM_005272547.4:c.99G>A	XP_005272604.1:p.Lys33=
XM_005272548.3:c.99G>A	XP_005272605.1:p.Lys33=
XM_005272550.3:c.99G>A	XP_005272607.1:p.Lys33=
XM_005272552.4:c.99G>A	XP_005272609.1:p.Lys33=
XM_005272553.5:c.99G>A	XP_005272610.1:p.Lys33=
XM_006720364.2:c.99G>A	XP_006720427.1:p.Lys33=
XM_006720365.3:c.99G>A	XP_006720428.1:p.Lys33=
XM_006720366.4:c.99G>A	XP_006720429.1:p.Lys33=
XM_011543877.2:c.99G>A	XP_011542179.1:p.Lys33=
XM_011543878.3:c.99G>A	XP_011542180.1:p.Lys33=
XM_011543879.3:c.99G>A	XP_011542181.1:p.Lys33=
XM_011543880.3:c.99G>A	XP_011542182.1:p.Lys33=
XM_017022645.1:c.99G>A	XP_016878134.1:p.Lys33=
XM_017022646.1:c.99G>A	XP_016878135.1:p.Lys33=
XM_017022647.1:c.99G>A	XP_016878136.1:p.Lys33=
XM_017022648.1:c.99G>A	XP_016878137.1:p.Lys33=
XM_017022649.2:c.99G>A	XP_016878138.1:p.Lys33=
XM_017022650.2:c.99G>A	XP_016878139.1:p.Lys33=
XM_017022651.2:c.99G>A	XP_016878140.1:p.Lys33=
XM_017022652.2:c.99G>A	XP_016878141.1:p.Lys33=
XM_017022653.2:c.99G>A	XP_016878142.1:p.Lys33=
XM_017022654.2:c.99G>A	XP_016878143.1:p.Lys33=
XM_017022655.1:c.99G>A	XP_016878144.1:p.Lys33=
XM_017022656.1:c.99G>A	XP_016878145.1:p.Lys33=
XM_017022657.1:c.99G>A	XP_016878146.1:p.Lys33=
XM_017022658.1:c.99G>A	XP_016878147.1:p.Lys33=
XM_017022659.1:c.99G>A	XP_016878148.1:p.Lys33=
XM_017022660.1:c.99G>A	XP_016878149.1:p.Lys33=
XM_017022661.1:c.99G>A	XP_016878150.1:p.Lys33=
XM_017022662.1:c.99G>A	XP_016878151.1:p.Lys33=
XM_017022663.1:c.99G>A	XP_016878152.1:p.Lys33=
XM_024450083.1:c.99G>A	XP_024305851.1:p.Lys33=
NM_001008860.3:c.99G>A	NP_001008860.1:p.Lys33=
NM_001008892.3:c.99G>A	NP_001008892.1:p.Lys33=
NM_001008894.3:c.99G>A	NP_001008894.1:p.Lys33=
NM_001184888.2:c.99G>A	NP_001171817.1:p.Lys33=
NM_001184889.2:c.99G>A	NP_001171818.1:p.Lys33=
NM_030922.7:c.99G>A MANE Select	NP_112184.4:p.Lys33=