Canonical Allele Identifier: CA371118366

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43037323C>A (hg19) ; chr8:g.43182180C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43182180C>A , CM000670.2:g.43182180C>A	GRCh38
NC_000008.10:g.43037323C>A , CM000670.1:g.43037323C>A	GRCh37
NC_000008.9:g.43156480C>A	NCBI36
NG_009552.1:g.46732C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1048C>A MANE Select	ENSP00000368965.4:p.Gln350Lys
ENST00000379644.8:c.1048C>A	ENSP00000368965.4:p.Gln350Lys
ENST00000519000.1:n.534C>A
ENST00000521576.1:c.199C>A	ENSP00000429029.1:p.Gln67Lys
ENST00000522082.5:c.289C>A	ENSP00000430151.1:p.Gln97Lys
ENST00000524016.5:c.152C>A
NM_152419.2:c.1048C>A	NP_689632.2:p.Gln350Lys
XM_005273409.1:c.1048C>A	XP_005273466.1:p.Gln350Lys
XM_005273410.1:c.1048C>A	XP_005273467.1:p.Gln350Lys
XM_005273411.1:c.856C>A	XP_005273468.1:p.Gln286Lys
XM_005273412.2:c.1048C>A	XP_005273469.1:p.Gln350Lys
NM_001363227.1:c.1048C>A	NP_001350156.1:p.Gln350Lys
NM_001363228.1:c.856C>A	NP_001350157.1:p.Gln286Lys
NM_001363229.1:c.184C>A	NP_001350158.1:p.Gln62Lys
XM_005273412.4:c.1048C>A	XP_005273469.1:p.Gln350Lys
NM_152419.3:c.1048C>A MANE Select	NP_689632.2:p.Gln350Lys
NM_001363227.2:c.1048C>A	NP_001350156.1:p.Gln350Lys
NM_001363228.2:c.856C>A	NP_001350157.1:p.Gln286Lys
NM_001363229.2:c.184C>A	NP_001350158.1:p.Gln62Lys