Canonical Allele Identifier: CA10358832

Gene: NHS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.17727638A>G , CM000685.2:g.17727638A>G	GRCh38
NC_000023.10:g.17745758A>G , CM000685.1:g.17745758A>G	GRCh37
NC_000023.9:g.17655679A>G	NCBI36
NG_011553.2:g.357219A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001291867.2:c.3532A>G MANE Select	NP_001278796.1:p.Ser1178Gly
ENST00000676302.1:c.3532A>G MANE Select	ENSP00000502262.1:p.Ser1178Gly
NM_001136024.3:c.3001A>G	NP_001129496.1:p.Ser1001Gly
NM_001136024.4:c.3001A>G	NP_001129496.1:p.Ser1001Gly
NM_001291867.1:c.3532A>G	NP_001278796.1:p.Ser1178Gly
NM_001291868.1:c.2938A>G	NP_001278797.1:p.Ser980Gly
NM_001291868.2:c.2938A>G	NP_001278797.1:p.Ser980Gly
NM_198270.3:c.3469A>G	NP_938011.1:p.Ser1157Gly
NM_198270.4:c.3469A>G	NP_938011.1:p.Ser1157Gly
ENST00000380060.7:c.3469A>G	ENSP00000369400.3:p.Ser1157Gly
ENST00000398097.7:c.3001A>G	ENSP00000381170.3:p.Ser1001Gly
ENST00000615422.1:c.2992A>G	ENSP00000480113.1:p.Ser998Gly
ENST00000615422.2:n.3927A>G
ENST00000617601.4:c.2920A>G	ENSP00000478433.1:p.Ser974Gly
ENST00000690608.1:n.2489A>G
XM_011545528.1:c.2584A>G	XP_011543830.1:p.Ser862Gly
XM_011545528.2:c.2584A>G	XP_011543830.1:p.Ser862Gly