Canonical Allele Identifier: CA460574605

Gene: HGSNAT

Linked Data

• gnomAD v4: 8-43140610-A-G
• MyVariant Identifiers: chr8:g.42995753A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140610A>G , CM000670.2:g.43140610A>G	GRCh38
NC_000008.10:g.42995753A>G , CM000670.1:g.42995753A>G	GRCh37
NC_000008.9:g.43114910A>G	NCBI36
NG_009552.1:g.5162A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.114A>G MANE Select	ENSP00000368965.4:p.Pro38=
ENST00000379644.8:c.114A>G	ENSP00000368965.4:p.Pro38=
ENST00000517319.1:c.114A>G	ENSP00000430032.1:p.Pro38=
ENST00000520704.1:c.-37A>G	ENSP00000429109.1:n.-37A>G
NM_152419.2:c.114A>G	NP_689632.2:p.Pro38=
XM_005273409.1:c.114A>G	XP_005273466.1:p.Pro38=
XM_005273410.1:c.114A>G	XP_005273467.1:p.Pro38=
XM_005273411.1:c.114A>G	XP_005273468.1:p.Pro38=
XM_005273412.2:c.114A>G	XP_005273469.1:p.Pro38=
NM_001363227.1:c.114A>G	NP_001350156.1:p.Pro38=
NM_001363228.1:c.114A>G	NP_001350157.1:p.Pro38=
NM_001363229.1:c.-720A>G	NP_001350158.1:n.-720A>G
XM_005273412.4:c.114A>G	XP_005273469.1:p.Pro38=
NM_152419.3:c.114A>G MANE Select	NP_689632.2:p.Pro38=
NM_001363227.2:c.114A>G	NP_001350156.1:p.Pro38=
NM_001363228.2:c.114A>G	NP_001350157.1:p.Pro38=
NM_001363229.2:c.-720A>G	NP_001350158.1:n.-720A>G