Canonical Allele Identifier: CA1779769332

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43173321T= , CM000670.2:g.43173321T=	GRCh38
NC_000008.10:g.43028464T= , CM000670.1:g.43028464T=	GRCh37
NC_000008.9:g.43147621T=	NCBI36
NG_009552.1:g.37873T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.821-392T= MANE Select	ENSP00000368965.4:n.821-392T=
ENST00000379644.8:c.821-392T=	ENSP00000368965.4:n.821-392T=
ENST00000520704.1:c.*270-392T=	ENSP00000429109.1:n.*270-392T=
ENST00000522082.5:c.62-392T=	ENSP00000430151.1:n.62-392T=
NM_152419.2:c.821-392T=	NP_689632.2:n.821-392T=
XM_005273409.1:c.821-392T=	XP_005273466.1:n.821-392T=
XM_005273410.1:c.821-392T=	XP_005273467.1:n.821-392T=
XM_005273411.1:c.820+935T=	XP_005273468.1:n.820+935T=
XM_005273412.2:c.821-392T=	XP_005273469.1:n.821-392T=
NM_001363227.1:c.821-392T=	NP_001350156.1:n.821-392T=
NM_001363228.1:c.820+935T=	NP_001350157.1:n.820+935T=
NM_001363229.1:c.-14+935T=	NP_001350158.1:n.-14+935T=
XM_005273412.4:c.821-392T=	XP_005273469.1:n.821-392T=
NM_152419.3:c.821-392T= MANE Select	NP_689632.2:n.821-392T=
NM_001363227.2:c.821-392T=	NP_001350156.1:n.821-392T=
NM_001363228.2:c.820+935T=	NP_001350157.1:n.820+935T=
NM_001363229.2:c.-14+935T=	NP_001350158.1:n.-14+935T=