Canonical Allele Identifier: CA371119593

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43047476A>T (hg19) ; chr8:g.43192333A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43192333A>T , CM000670.2:g.43192333A>T	GRCh38
NC_000008.10:g.43047476A>T , CM000670.1:g.43047476A>T	GRCh37
NC_000008.9:g.43166633A>T	NCBI36
NG_009552.1:g.56885A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1280A>T MANE Select	ENSP00000368965.4:p.Asp427Val
ENST00000379644.8:c.1280A>T	ENSP00000368965.4:p.Asp427Val
ENST00000520678.1:n.213A>T
ENST00000521576.1:c.431A>T	ENSP00000429029.1:p.Asp144Val
ENST00000524016.5:c.384A>T
NM_152419.2:c.1280A>T	NP_689632.2:p.Asp427Val
XM_005273409.1:c.1280A>T	XP_005273466.1:p.Asp427Val
XM_005273410.1:c.1280A>T	XP_005273467.1:p.Asp427Val
XM_005273411.1:c.1088A>T	XP_005273468.1:p.Asp363Val
XM_005273412.2:c.1280A>T	XP_005273469.1:p.Asp427Val
NM_001363227.1:c.1280A>T	NP_001350156.1:p.Asp427Val
NM_001363228.1:c.1088A>T	NP_001350157.1:p.Asp363Val
NM_001363229.1:c.416A>T	NP_001350158.1:p.Asp139Val
XM_005273412.4:c.1280A>T	XP_005273469.1:p.Asp427Val
NM_152419.3:c.1280A>T MANE Select	NP_689632.2:p.Asp427Val
NM_001363227.2:c.1280A>T	NP_001350156.1:p.Asp427Val
NM_001363228.2:c.1088A>T	NP_001350157.1:p.Asp363Val
NM_001363229.2:c.416A>T	NP_001350158.1:p.Asp139Val