Canonical Allele Identifier: CA4736833
Community Standard Title: NM_152419.3(HGSNAT):c.1270G>A (p.Gly424Ser)
Gene: HGSNAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43192323G>A , CM000670.2:g.43192323G>A GRCh38
NC_000008.10:g.43047466G>A , CM000670.1:g.43047466G>A GRCh37
NC_000008.9:g.43166623G>A NCBI36
NG_009552.1:g.56875G>A

Transcript Alleles

HGVS Amino-acid Change
NM_152419.3:c.1270G>A MANE Select NP_689632.2:p.Gly424Ser
ENST00000379644.9:c.1270G>A MANE Select ENSP00000368965.4:p.Gly424Ser
NM_001363227.1:c.1270G>A NP_001350156.1:p.Gly424Ser
NM_001363227.2:c.1270G>A NP_001350156.1:p.Gly424Ser
NM_001363228.1:c.1078G>A NP_001350157.1:p.Gly360Ser
NM_001363228.2:c.1078G>A NP_001350157.1:p.Gly360Ser
NM_001363229.1:c.406G>A NP_001350158.1:p.Gly136Ser
NM_001363229.2:c.406G>A NP_001350158.1:p.Gly136Ser
NM_152419.2:c.1270G>A NP_689632.2:p.Gly424Ser
ENST00000379644.8:c.1270G>A ENSP00000368965.4:p.Gly424Ser
ENST00000520678.1:n.203G>A
ENST00000521576.1:c.421G>A ENSP00000429029.1:p.Gly141Ser
ENST00000524016.5:c.374G>A
XM_005273409.1:c.1270G>A XP_005273466.1:p.Gly424Ser
XM_005273410.1:c.1270G>A XP_005273467.1:p.Gly424Ser
XM_005273411.1:c.1078G>A XP_005273468.1:p.Gly360Ser
XM_005273412.2:c.1270G>A XP_005273469.1:p.Gly424Ser
XM_005273412.4:c.1270G>A XP_005273469.1:p.Gly424Ser