Canonical Allele Identifier: CA1779774329
Gene: HGSNAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43182093G= , CM000670.2:g.43182093G= GRCh38
NC_000008.10:g.43037236G= , CM000670.1:g.43037236G= GRCh37
NC_000008.9:g.43156393G= NCBI36
NG_009552.1:g.46645G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379644.9:c.1013-52G= MANE Select ENSP00000368965.4:n.1013-52G=
ENST00000379644.8:c.1013-52G= ENSP00000368965.4:n.1013-52G=
ENST00000519000.1:n.447G=
ENST00000521576.1:c.164-52G= ENSP00000429029.1:n.164-52G=
ENST00000522082.5:c.254-52G= ENSP00000430151.1:n.254-52G=
ENST00000524016.5:c.117-52G=
NM_152419.2:c.1013-52G= NP_689632.2:n.1013-52G=
XM_005273409.1:c.1013-52G= XP_005273466.1:n.1013-52G=
XM_005273410.1:c.1013-52G= XP_005273467.1:n.1013-52G=
XM_005273411.1:c.821-52G= XP_005273468.1:n.821-52G=
XM_005273412.2:c.1013-52G= XP_005273469.1:n.1013-52G=
NM_001363227.1:c.1013-52G= NP_001350156.1:n.1013-52G=
NM_001363228.1:c.821-52G= NP_001350157.1:n.821-52G=
NM_001363229.1:c.149-52G= NP_001350158.1:n.149-52G=
XM_005273412.4:c.1013-52G= XP_005273469.1:n.1013-52G=
NM_152419.3:c.1013-52G= MANE Select NP_689632.2:n.1013-52G=
NM_001363227.2:c.1013-52G= NP_001350156.1:n.1013-52G=
NM_001363228.2:c.821-52G= NP_001350157.1:n.821-52G=
NM_001363229.2:c.149-52G= NP_001350158.1:n.149-52G=