Canonical Allele Identifier: CA1726545780
Gene: GNGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93909096T= , CM000669.2:g.93909096T= GRCh38
NC_000007.13:g.93538408T= , CM000669.1:g.93538408T= GRCh37
NC_000007.12:g.93376344T= NCBI36
NG_051196.1:g.7589T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248572.10:c.97-1694T= MANE Select ENSP00000248572.5:n.97-1694T=
ENST00000248572.9:c.97-1694T= ENSP00000248572.5:n.97-1694T=
ENST00000428834.1:c.97-387T= ENSP00000401781.1:n.97-387T=
ENST00000429473.1:c.97-1694T= ENSP00000388777.1:n.97-1694T=
ENST00000430875.1:c.97-387T= ENSP00000395756.1:n.97-387T=
ENST00000455502.5:c.97-387T= ENSP00000395857.1:n.97-387T=
NM_021955.3:c.97-1694T= NP_068774.1:n.97-1694T=
NM_001329426.1:c.97-1694T= NP_001316355.1:n.97-1694T=
NM_021955.4:c.97-1694T= NP_068774.1:n.97-1694T=
NM_001329426.2:c.97-1694T= NP_001316355.1:n.97-1694T=
NM_021955.5:c.97-1694T= MANE Select NP_068774.1:n.97-1694T=