Canonical Allele Identifier: CA1779749756

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140614G= , CM000670.2:g.43140614G=	GRCh38
NC_000008.10:g.42995757G= , CM000670.1:g.42995757G=	GRCh37
NC_000008.9:g.43114914G=	NCBI36
NG_009552.1:g.5166G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.118G= MANE Select	ENSP00000368965.4:p.Asp40=
ENST00000379644.8:c.118G=	ENSP00000368965.4:p.Asp40=
ENST00000517319.1:c.118G=	ENSP00000430032.1:p.Asp40=
ENST00000520704.1:c.-33G=	ENSP00000429109.1:n.-33G=
NM_152419.2:c.118G=	NP_689632.2:p.Asp40=
XM_005273409.1:c.118G=	XP_005273466.1:p.Asp40=
XM_005273410.1:c.118G=	XP_005273467.1:p.Asp40=
XM_005273411.1:c.118G=	XP_005273468.1:p.Asp40=
XM_005273412.2:c.118G=	XP_005273469.1:p.Asp40=
NM_001363227.1:c.118G=	NP_001350156.1:p.Asp40=
NM_001363228.1:c.118G=	NP_001350157.1:p.Asp40=
NM_001363229.1:c.-716G=	NP_001350158.1:n.-716G=
XM_005273412.4:c.118G=	XP_005273469.1:p.Asp40=
NM_152419.3:c.118G= MANE Select	NP_689632.2:p.Asp40=
NM_001363227.2:c.118G=	NP_001350156.1:p.Asp40=
NM_001363228.2:c.118G=	NP_001350157.1:p.Asp40=
NM_001363229.2:c.-716G=	NP_001350158.1:n.-716G=