Canonical Allele Identifier: CA1779749645

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140470G= , CM000670.2:g.43140470G=	GRCh38
NC_000008.10:g.42995613G= , CM000670.1:g.42995613G=	GRCh37
NC_000008.9:g.43114770G=	NCBI36
NG_009552.1:g.5022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.-27G= MANE Select	ENSP00000368965.4:n.-27G=
ENST00000379644.8:c.-27G=	ENSP00000368965.4:n.-27G=
NM_152419.2:c.-27G=	NP_689632.2:n.-27G=
XM_005273409.1:c.-27G=	XP_005273466.1:n.-27G=
XM_005273410.1:c.-27G=	XP_005273467.1:n.-27G=
XM_005273411.1:c.-27G=	XP_005273468.1:n.-27G=
XM_005273412.2:c.-27G=	XP_005273469.1:n.-27G=
NM_001363227.1:c.-27G=	NP_001350156.1:n.-27G=
NM_001363228.1:c.-27G=	NP_001350157.1:n.-27G=
NM_001363229.1:c.-860G=	NP_001350158.1:n.-860G=
XM_005273412.4:c.-27G=	XP_005273469.1:n.-27G=
NM_152419.3:c.-27G= MANE Select	NP_689632.2:n.-27G=
NM_001363227.2:c.-27G=	NP_001350156.1:n.-27G=
NM_001363228.2:c.-27G=	NP_001350157.1:n.-27G=
NM_001363229.2:c.-860G=	NP_001350158.1:n.-860G=