Canonical Allele Identifier: CA460574600

Gene: HGSNAT

Linked Data

• gnomAD v4: 8-43140607-G-T
• MyVariant Identifiers: chr8:g.42995750G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140607G>T , CM000670.2:g.43140607G>T	GRCh38
NC_000008.10:g.42995750G>T , CM000670.1:g.42995750G>T	GRCh37
NC_000008.9:g.43114907G>T	NCBI36
NG_009552.1:g.5159G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.111G>T MANE Select	ENSP00000368965.4:p.Pro37=
ENST00000379644.8:c.111G>T	ENSP00000368965.4:p.Pro37=
ENST00000517319.1:c.111G>T	ENSP00000430032.1:p.Pro37=
ENST00000520704.1:c.-40G>T	ENSP00000429109.1:n.-40G>T
NM_152419.2:c.111G>T	NP_689632.2:p.Pro37=
XM_005273409.1:c.111G>T	XP_005273466.1:p.Pro37=
XM_005273410.1:c.111G>T	XP_005273467.1:p.Pro37=
XM_005273411.1:c.111G>T	XP_005273468.1:p.Pro37=
XM_005273412.2:c.111G>T	XP_005273469.1:p.Pro37=
NM_001363227.1:c.111G>T	NP_001350156.1:p.Pro37=
NM_001363228.1:c.111G>T	NP_001350157.1:p.Pro37=
NM_001363229.1:c.-723G>T	NP_001350158.1:n.-723G>T
XM_005273412.4:c.111G>T	XP_005273469.1:p.Pro37=
NM_152419.3:c.111G>T MANE Select	NP_689632.2:p.Pro37=
NM_001363227.2:c.111G>T	NP_001350156.1:p.Pro37=
NM_001363228.2:c.111G>T	NP_001350157.1:p.Pro37=
NM_001363229.2:c.-723G>T	NP_001350158.1:n.-723G>T