Canonical Allele Identifier: CA412360087

Gene: NHS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.17726820A>G , CM000685.2:g.17726820A>G	GRCh38
NC_000023.10:g.17744940A>G , CM000685.1:g.17744940A>G	GRCh37
NC_000023.9:g.17654861A>G	NCBI36
NG_011553.2:g.356401A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001291867.2:c.2714A>G MANE Select	NP_001278796.1:p.Asn905Ser
ENST00000676302.1:c.2714A>G MANE Select	ENSP00000502262.1:p.Asn905Ser
NM_001136024.3:c.2183A>G	NP_001129496.1:p.Asn728Ser
NM_001136024.4:c.2183A>G	NP_001129496.1:p.Asn728Ser
NM_001291867.1:c.2714A>G	NP_001278796.1:p.Asn905Ser
NM_001291868.1:c.2120A>G	NP_001278797.1:p.Asn707Ser
NM_001291868.2:c.2120A>G	NP_001278797.1:p.Asn707Ser
NM_198270.3:c.2651A>G	NP_938011.1:p.Asn884Ser
NM_198270.4:c.2651A>G	NP_938011.1:p.Asn884Ser
ENST00000380060.7:c.2651A>G	ENSP00000369400.3:p.Asn884Ser
ENST00000398097.7:c.2183A>G	ENSP00000381170.3:p.Asn728Ser
ENST00000615422.1:c.2174A>G	ENSP00000480113.1:p.Asn725Ser
ENST00000615422.2:n.3109A>G
ENST00000617601.4:c.2102A>G	ENSP00000478433.1:p.Asn701Ser
ENST00000690608.1:n.1671A>G
XM_011545528.1:c.1766A>G	XP_011543830.1:p.Asn589Ser
XM_011545528.2:c.1766A>G	XP_011543830.1:p.Asn589Ser