Canonical Allele Identifier: CA371118336

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43037306G>C (hg19) ; chr8:g.43182163G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43182163G>C , CM000670.2:g.43182163G>C	GRCh38
NC_000008.10:g.43037306G>C , CM000670.1:g.43037306G>C	GRCh37
NC_000008.9:g.43156463G>C	NCBI36
NG_009552.1:g.46715G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1031G>C MANE Select	ENSP00000368965.4:p.Arg344Pro
ENST00000379644.8:c.1031G>C	ENSP00000368965.4:p.Arg344Pro
ENST00000519000.1:n.517G>C
ENST00000521576.1:c.182G>C	ENSP00000429029.1:p.Arg61Pro
ENST00000522082.5:c.272G>C	ENSP00000430151.1:p.Arg91Pro
ENST00000524016.5:c.135G>C
NM_152419.2:c.1031G>C	NP_689632.2:p.Arg344Pro
XM_005273409.1:c.1031G>C	XP_005273466.1:p.Arg344Pro
XM_005273410.1:c.1031G>C	XP_005273467.1:p.Arg344Pro
XM_005273411.1:c.839G>C	XP_005273468.1:p.Arg280Pro
XM_005273412.2:c.1031G>C	XP_005273469.1:p.Arg344Pro
NM_001363227.1:c.1031G>C	NP_001350156.1:p.Arg344Pro
NM_001363228.1:c.839G>C	NP_001350157.1:p.Arg280Pro
NM_001363229.1:c.167G>C	NP_001350158.1:p.Arg56Pro
XM_005273412.4:c.1031G>C	XP_005273469.1:p.Arg344Pro
NM_152419.3:c.1031G>C MANE Select	NP_689632.2:p.Arg344Pro
NM_001363227.2:c.1031G>C	NP_001350156.1:p.Arg344Pro
NM_001363228.2:c.839G>C	NP_001350157.1:p.Arg280Pro
NM_001363229.2:c.167G>C	NP_001350158.1:p.Arg56Pro