Canonical Allele Identifier: CA1779749628

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140460C= , CM000670.2:g.43140460C=	GRCh38
NC_000008.10:g.42995603C= , CM000670.1:g.42995603C=	GRCh37
NC_000008.9:g.43114760C=	NCBI36
NG_009552.1:g.5012C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.8:c.-37C=	ENSP00000368965.4:n.-37C=
NM_152419.2:c.-37C=	NP_689632.2:n.-37C=
XM_005273409.1:c.-37C=	XP_005273466.1:n.-37C=
XM_005273410.1:c.-37C=	XP_005273467.1:n.-37C=
XM_005273411.1:c.-37C=	XP_005273468.1:n.-37C=
XM_005273412.2:c.-37C=	XP_005273469.1:n.-37C=
XM_005273412.4:c.-37C=	XP_005273469.1:n.-37C=