Canonical Allele Identifier: CA1726545716
Gene: GNGT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93909004C= , CM000669.2:g.93909004C= GRCh38
NC_000007.13:g.93538316C= , CM000669.1:g.93538316C= GRCh37
NC_000007.12:g.93376252C= NCBI36
NG_051196.1:g.7497C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248572.10:c.97-1786C= MANE Select ENSP00000248572.5:n.97-1786C=
ENST00000248572.9:c.97-1786C= ENSP00000248572.5:n.97-1786C=
ENST00000428834.1:c.97-479C= ENSP00000401781.1:n.97-479C=
ENST00000429473.1:c.97-1786C= ENSP00000388777.1:n.97-1786C=
ENST00000430875.1:c.97-479C= ENSP00000395756.1:n.97-479C=
ENST00000455502.5:c.97-479C= ENSP00000395857.1:n.97-479C=
NM_021955.3:c.97-1786C= NP_068774.1:n.97-1786C=
NM_001329426.1:c.97-1786C= NP_001316355.1:n.97-1786C=
NM_021955.4:c.97-1786C= NP_068774.1:n.97-1786C=
NM_001329426.2:c.97-1786C= NP_001316355.1:n.97-1786C=
NM_021955.5:c.97-1786C= MANE Select NP_068774.1:n.97-1786C=
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