Canonical Allele Identifier: CA176073813
Gene: HGSNAT HGNC NCBI

Linked Data

dbSNP Id: rs1034080389

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43192085T>C , CM000670.2:g.43192085T>C GRCh38
NC_000008.10:g.43047228T>C , CM000670.1:g.43047228T>C GRCh37
NC_000008.9:g.43166385T>C NCBI36
NG_009552.1:g.56637T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379644.9:c.1251-219T>C MANE Select ENSP00000368965.4:n.1251-219T>C
ENST00000379644.8:c.1251-219T>C ENSP00000368965.4:n.1251-219T>C
ENST00000520678.1:n.184-219T>C
ENST00000521576.1:c.402-219T>C ENSP00000429029.1:n.402-219T>C
ENST00000524016.5:c.355-219T>C
NM_152419.2:c.1251-219T>C NP_689632.2:n.1251-219T>C
XM_005273409.1:c.1251-219T>C XP_005273466.1:n.1251-219T>C
XM_005273410.1:c.1251-219T>C XP_005273467.1:n.1251-219T>C
XM_005273411.1:c.1059-219T>C XP_005273468.1:n.1059-219T>C
XM_005273412.2:c.1251-219T>C XP_005273469.1:n.1251-219T>C
NM_001363227.1:c.1251-219T>C NP_001350156.1:n.1251-219T>C
NM_001363228.1:c.1059-219T>C NP_001350157.1:n.1059-219T>C
NM_001363229.1:c.387-219T>C NP_001350158.1:n.387-219T>C
XM_005273412.4:c.1251-219T>C XP_005273469.1:n.1251-219T>C
NM_152419.3:c.1251-219T>C MANE Select NP_689632.2:n.1251-219T>C
NM_001363227.2:c.1251-219T>C NP_001350156.1:n.1251-219T>C
NM_001363228.2:c.1059-219T>C NP_001350157.1:n.1059-219T>C
NM_001363229.2:c.387-219T>C NP_001350158.1:n.387-219T>C