Canonical Allele Identifier: CA1779778010
Gene: HGSNAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43200608T= , CM000670.2:g.43200608T= GRCh38
NC_000008.10:g.43055751T= , CM000670.1:g.43055751T= GRCh37
NC_000008.9:g.43174908T= NCBI36
NG_009552.1:g.65160T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379644.9:c.*1039T= MANE Select ENSP00000368965.4:n.*1039T=
ENST00000379644.8:c.*1039T= ENSP00000368965.4:n.*1039T=
NM_152419.2:c.*1039T= NP_689632.2:n.*1039T=
XM_005273409.1:c.*1039T= XP_005273466.1:n.*1039T=
XM_005273410.1:c.*1039T= XP_005273467.1:n.*1039T=
XM_005273411.1:c.*1039T= XP_005273468.1:n.*1039T=
NM_001363227.1:c.*1039T= NP_001350156.1:n.*1039T=
NM_001363228.1:c.*1039T= NP_001350157.1:n.*1039T=
NM_001363229.1:c.*1039T= NP_001350158.1:n.*1039T=
NM_152419.3:c.*1039T= MANE Select NP_689632.2:n.*1039T=
NM_001363227.2:c.*1039T= NP_001350156.1:n.*1039T=
NM_001363228.2:c.*1039T= NP_001350157.1:n.*1039T=
NM_001363229.2:c.*1039T= NP_001350158.1:n.*1039T=