Canonical Allele Identifier: CA1779774288
Gene: HGSNAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43182003A= , CM000670.2:g.43182003A= GRCh38
NC_000008.10:g.43037146A= , CM000670.1:g.43037146A= GRCh37
NC_000008.9:g.43156303A= NCBI36
NG_009552.1:g.46555A=

Transcript Alleles

HGVS Amino-acid change
ENST00000379644.9:c.1013-142A= MANE Select ENSP00000368965.4:n.1013-142A=
ENST00000379644.8:c.1013-142A= ENSP00000368965.4:n.1013-142A=
ENST00000519000.1:n.357A=
ENST00000521576.1:c.164-142A= ENSP00000429029.1:n.164-142A=
ENST00000522082.5:c.254-142A= ENSP00000430151.1:n.254-142A=
ENST00000524016.5:c.117-142A=
NM_152419.2:c.1013-142A= NP_689632.2:n.1013-142A=
XM_005273409.1:c.1013-142A= XP_005273466.1:n.1013-142A=
XM_005273410.1:c.1013-142A= XP_005273467.1:n.1013-142A=
XM_005273411.1:c.821-142A= XP_005273468.1:n.821-142A=
XM_005273412.2:c.1013-142A= XP_005273469.1:n.1013-142A=
NM_001363227.1:c.1013-142A= NP_001350156.1:n.1013-142A=
NM_001363228.1:c.821-142A= NP_001350157.1:n.821-142A=
NM_001363229.1:c.149-142A= NP_001350158.1:n.149-142A=
XM_005273412.4:c.1013-142A= XP_005273469.1:n.1013-142A=
NM_152419.3:c.1013-142A= MANE Select NP_689632.2:n.1013-142A=
NM_001363227.2:c.1013-142A= NP_001350156.1:n.1013-142A=
NM_001363228.2:c.821-142A= NP_001350157.1:n.821-142A=
NM_001363229.2:c.149-142A= NP_001350158.1:n.149-142A=