Canonical Allele Identifier: CA278815

Gene: NHS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.17726876del , CM000685.2:g.17726876del	GRCh38
NC_000023.10:g.17744996del , CM000685.1:g.17744996del	GRCh37
NC_000023.9:g.17654917del	NCBI36
NG_011553.2:g.356457del

Transcript Alleles

HGVS	Amino-acid Change
NM_001291867.2:c.2770del MANE Select	NP_001278796.1:p.Glu924AsnfsTer4
ENST00000676302.1:c.2770del MANE Select	ENSP00000502262.1:p.Glu924AsnfsTer4
NM_001136024.3:c.2239del	NP_001129496.1:p.Glu747AsnfsTer4
NM_001136024.4:c.2239del	NP_001129496.1:p.Glu747AsnfsTer4
NM_001291867.1:c.2770del	NP_001278796.1:p.Glu924AsnfsTer4
NM_001291868.1:c.2176del	NP_001278797.1:p.Glu726AsnfsTer4
NM_001291868.2:c.2176del	NP_001278797.1:p.Glu726AsnfsTer4
NM_198270.3:c.2707del	NP_938011.1:p.Glu903AsnfsTer4
NM_198270.4:c.2707del	NP_938011.1:p.Glu903AsnfsTer4
ENST00000380060.7:c.2707del	ENSP00000369400.3:p.Glu903AsnfsTer4
ENST00000398097.7:c.2239del	ENSP00000381170.3:p.Glu747AsnfsTer4
ENST00000615422.1:c.2230del	ENSP00000480113.1:p.Glu744AsnfsTer4
ENST00000615422.2:n.3165del
ENST00000617601.4:c.2158del	ENSP00000478433.1:p.Glu720AsnfsTer4
ENST00000690608.1:n.1727del
XM_011545528.1:c.1822del	XP_011543830.1:p.Glu608AsnfsTer4
XM_011545528.2:c.1822del	XP_011543830.1:p.Glu608AsnfsTer4