Canonical Allele Identifier: CA1779749638

Gene: HGSNAT

Linked Data

• dbSNP Id: rs1165264908
• gnomAD v4: 8-43140466-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140466G>T , CM000670.2:g.43140466G>T	GRCh38
NC_000008.10:g.42995609G>T , CM000670.1:g.42995609G>T	GRCh37
NC_000008.9:g.43114766G>T	NCBI36
NG_009552.1:g.5018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.-31G>T MANE Select	ENSP00000368965.4:n.-31G>T
ENST00000379644.8:c.-31G>T	ENSP00000368965.4:n.-31G>T
NM_152419.2:c.-31G>T	NP_689632.2:n.-31G>T
XM_005273409.1:c.-31G>T	XP_005273466.1:n.-31G>T
XM_005273410.1:c.-31G>T	XP_005273467.1:n.-31G>T
XM_005273411.1:c.-31G>T	XP_005273468.1:n.-31G>T
XM_005273412.2:c.-31G>T	XP_005273469.1:n.-31G>T
NM_001363227.1:c.-31G>T	NP_001350156.1:n.-31G>T
NM_001363228.1:c.-31G>T	NP_001350157.1:n.-31G>T
NM_001363229.1:c.-864G>T	NP_001350158.1:n.-864G>T
XM_005273412.4:c.-31G>T	XP_005273469.1:n.-31G>T
NM_152419.3:c.-31G>T MANE Select	NP_689632.2:n.-31G>T
NM_001363227.2:c.-31G>T	NP_001350156.1:n.-31G>T
NM_001363228.2:c.-31G>T	NP_001350157.1:n.-31G>T
NM_001363229.2:c.-864G>T	NP_001350158.1:n.-864G>T