Canonical Allele Identifier: CA326968100

Gene: NHS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.17728193A>G , CM000685.2:g.17728193A>G	GRCh38
NC_000023.10:g.17746313A>G , CM000685.1:g.17746313A>G	GRCh37
NC_000023.9:g.17656234A>G	NCBI36
NG_011553.2:g.357774A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001291867.2:c.4087A>G MANE Select	NP_001278796.1:p.Ile1363Val
ENST00000676302.1:c.4087A>G MANE Select	ENSP00000502262.1:p.Ile1363Val
NM_001136024.3:c.3556A>G	NP_001129496.1:p.Ile1186Val
NM_001136024.4:c.3556A>G	NP_001129496.1:p.Ile1186Val
NM_001291867.1:c.4087A>G	NP_001278796.1:p.Ile1363Val
NM_001291868.1:c.3493A>G	NP_001278797.1:p.Ile1165Val
NM_001291868.2:c.3493A>G	NP_001278797.1:p.Ile1165Val
NM_198270.3:c.4024A>G	NP_938011.1:p.Ile1342Val
NM_198270.4:c.4024A>G	NP_938011.1:p.Ile1342Val
ENST00000380060.7:c.4024A>G	ENSP00000369400.3:p.Ile1342Val
ENST00000398097.7:c.3556A>G	ENSP00000381170.3:p.Ile1186Val
ENST00000615422.1:c.3547A>G	ENSP00000480113.1:p.Ile1183Val
ENST00000615422.2:n.4482A>G
ENST00000617601.4:c.3475A>G	ENSP00000478433.1:p.Ile1159Val
ENST00000690608.1:n.3044A>G
XM_011545528.1:c.3139A>G	XP_011543830.1:p.Ile1047Val
XM_011545528.2:c.3139A>G	XP_011543830.1:p.Ile1047Val