Canonical Allele Identifier: CA1779749755
Gene: HGSNAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43140613A= , CM000670.2:g.43140613A= GRCh38
NC_000008.10:g.42995756A= , CM000670.1:g.42995756A= GRCh37
NC_000008.9:g.43114913A= NCBI36
NG_009552.1:g.5165A=

Transcript Alleles

HGVS Amino-acid change
ENST00000379644.9:c.117A= MANE Select ENSP00000368965.4:p.Arg39=
ENST00000379644.8:c.117A= ENSP00000368965.4:p.Arg39=
ENST00000517319.1:c.117A= ENSP00000430032.1:p.Arg39=
ENST00000520704.1:c.-34A= ENSP00000429109.1:n.-34A=
NM_152419.2:c.117A= NP_689632.2:p.Arg39=
XM_005273409.1:c.117A= XP_005273466.1:p.Arg39=
XM_005273410.1:c.117A= XP_005273467.1:p.Arg39=
XM_005273411.1:c.117A= XP_005273468.1:p.Arg39=
XM_005273412.2:c.117A= XP_005273469.1:p.Arg39=
NM_001363227.1:c.117A= NP_001350156.1:p.Arg39=
NM_001363228.1:c.117A= NP_001350157.1:p.Arg39=
NM_001363229.1:c.-717A= NP_001350158.1:n.-717A=
XM_005273412.4:c.117A= XP_005273469.1:p.Arg39=
NM_152419.3:c.117A= MANE Select NP_689632.2:p.Arg39=
NM_001363227.2:c.117A= NP_001350156.1:p.Arg39=
NM_001363228.2:c.117A= NP_001350157.1:p.Arg39=
NM_001363229.2:c.-717A= NP_001350158.1:n.-717A=