Canonical Allele Identifier: CA460578140

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43047462T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43192319T>A , CM000670.2:g.43192319T>A	GRCh38
NC_000008.10:g.43047462T>A , CM000670.1:g.43047462T>A	GRCh37
NC_000008.9:g.43166619T>A	NCBI36
NG_009552.1:g.56871T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1266T>A MANE Select	ENSP00000368965.4:p.Pro422=
ENST00000379644.8:c.1266T>A	ENSP00000368965.4:p.Pro422=
ENST00000520678.1:n.199T>A
ENST00000521576.1:c.417T>A	ENSP00000429029.1:p.Pro139=
ENST00000524016.5:c.370T>A
NM_152419.2:c.1266T>A	NP_689632.2:p.Pro422=
XM_005273409.1:c.1266T>A	XP_005273466.1:p.Pro422=
XM_005273410.1:c.1266T>A	XP_005273467.1:p.Pro422=
XM_005273411.1:c.1074T>A	XP_005273468.1:p.Pro358=
XM_005273412.2:c.1266T>A	XP_005273469.1:p.Pro422=
NM_001363227.1:c.1266T>A	NP_001350156.1:p.Pro422=
NM_001363228.1:c.1074T>A	NP_001350157.1:p.Pro358=
NM_001363229.1:c.402T>A	NP_001350158.1:p.Pro134=
XM_005273412.4:c.1266T>A	XP_005273469.1:p.Pro422=
NM_152419.3:c.1266T>A MANE Select	NP_689632.2:p.Pro422=
NM_001363227.2:c.1266T>A	NP_001350156.1:p.Pro422=
NM_001363228.2:c.1074T>A	NP_001350157.1:p.Pro358=
NM_001363229.2:c.402T>A	NP_001350158.1:p.Pro134=