Canonical Allele Identifier: CA4736836

Gene: HGSNAT

Linked Data

• ClinVar Variation Id: 1144186
• ClinVar RCV Id: RCV001482587
• dbSNP Id: rs748987930
• ExAC: 8:43047486 G / A
• gnomAD v2: 8-43047486-G-A
• gnomAD v3: 8-43192343-G-A
• gnomAD v4: 8-43192343-G-A
• MyVariant Identifiers: chr8:g.43047486G>A (hg19) ; chr8:g.43192343G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43192343G>A , CM000670.2:g.43192343G>A	GRCh38
NC_000008.10:g.43047486G>A , CM000670.1:g.43047486G>A	GRCh37
NC_000008.9:g.43166643G>A	NCBI36
NG_009552.1:g.56895G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1290G>A MANE Select	ENSP00000368965.4:p.Lys430=
ENST00000379644.8:c.1290G>A	ENSP00000368965.4:p.Lys430=
ENST00000520678.1:n.223G>A
ENST00000521576.1:c.441G>A	ENSP00000429029.1:p.Lys147=
ENST00000524016.5:c.394G>A
NM_152419.2:c.1290G>A	NP_689632.2:p.Lys430=
XM_005273409.1:c.1290G>A	XP_005273466.1:p.Lys430=
XM_005273410.1:c.1290G>A	XP_005273467.1:p.Lys430=
XM_005273411.1:c.1098G>A	XP_005273468.1:p.Lys366=
XM_005273412.2:c.1290G>A	XP_005273469.1:p.Lys430=
NM_001363227.1:c.1290G>A	NP_001350156.1:p.Lys430=
NM_001363228.1:c.1098G>A	NP_001350157.1:p.Lys366=
NM_001363229.1:c.426G>A	NP_001350158.1:p.Lys142=
XM_005273412.4:c.1290G>A	XP_005273469.1:p.Lys430=
NM_152419.3:c.1290G>A MANE Select	NP_689632.2:p.Lys430=
NM_001363227.2:c.1290G>A	NP_001350156.1:p.Lys430=
NM_001363228.2:c.1098G>A	NP_001350157.1:p.Lys366=
NM_001363229.2:c.426G>A	NP_001350158.1:p.Lys142=