Canonical Allele Identifier: CA412350911

Gene: NHS

Linked Data

• MyVariant Identifiers: chrX:g.17743553G>C (hg19) ; chrX:g.17725433G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.17725433G>C , CM000685.2:g.17725433G>C	GRCh38
NC_000023.10:g.17743553G>C , CM000685.1:g.17743553G>C	GRCh37
NC_000023.9:g.17653474G>C	NCBI36
NG_011553.2:g.355014G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615422.2:n.1722G>C
ENST00000690213.1:n.3207G>C
ENST00000690608.1:n.284G>C
ENST00000676302.1:c.1327G>C MANE Select	ENSP00000502262.1:p.Gly443Arg
ENST00000380060.7:c.1264G>C	ENSP00000369400.3:p.Gly422Arg
ENST00000398097.7:c.796G>C	ENSP00000381170.3:p.Gly266Arg
ENST00000615422.1:c.787G>C	ENSP00000480113.1:p.Gly263Arg
ENST00000617601.4:c.715G>C	ENSP00000478433.1:p.Gly239Arg
NM_001136024.3:c.796G>C	NP_001129496.1:p.Gly266Arg
NM_001291867.1:c.1327G>C	NP_001278796.1:p.Gly443Arg
NM_001291868.1:c.733G>C	NP_001278797.1:p.Gly245Arg
NM_198270.3:c.1264G>C	NP_938011.1:p.Gly422Arg
XM_011545528.1:c.379G>C	XP_011543830.1:p.Gly127Arg
XM_011545528.2:c.379G>C	XP_011543830.1:p.Gly127Arg
NM_001136024.4:c.796G>C	NP_001129496.1:p.Gly266Arg
NM_001291867.2:c.1327G>C MANE Select	NP_001278796.1:p.Gly443Arg
NM_001291868.2:c.733G>C	NP_001278797.1:p.Gly245Arg
NM_198270.4:c.1264G>C	NP_938011.1:p.Gly422Arg