Canonical Allele Identifier: CA460574660

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43037313T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43182170T>G , CM000670.2:g.43182170T>G	GRCh38
NC_000008.10:g.43037313T>G , CM000670.1:g.43037313T>G	GRCh37
NC_000008.9:g.43156470T>G	NCBI36
NG_009552.1:g.46722T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1038T>G MANE Select	ENSP00000368965.4:p.Pro346=
ENST00000379644.8:c.1038T>G	ENSP00000368965.4:p.Pro346=
ENST00000519000.1:n.524T>G
ENST00000521576.1:c.189T>G	ENSP00000429029.1:p.Pro63=
ENST00000522082.5:c.279T>G	ENSP00000430151.1:p.Pro93=
ENST00000524016.5:c.142T>G
NM_152419.2:c.1038T>G	NP_689632.2:p.Pro346=
XM_005273409.1:c.1038T>G	XP_005273466.1:p.Pro346=
XM_005273410.1:c.1038T>G	XP_005273467.1:p.Pro346=
XM_005273411.1:c.846T>G	XP_005273468.1:p.Pro282=
XM_005273412.2:c.1038T>G	XP_005273469.1:p.Pro346=
NM_001363227.1:c.1038T>G	NP_001350156.1:p.Pro346=
NM_001363228.1:c.846T>G	NP_001350157.1:p.Pro282=
NM_001363229.1:c.174T>G	NP_001350158.1:p.Pro58=
XM_005273412.4:c.1038T>G	XP_005273469.1:p.Pro346=
NM_152419.3:c.1038T>G MANE Select	NP_689632.2:p.Pro346=
NM_001363227.2:c.1038T>G	NP_001350156.1:p.Pro346=
NM_001363228.2:c.846T>G	NP_001350157.1:p.Pro282=
NM_001363229.2:c.174T>G	NP_001350158.1:p.Pro58=