Canonical Allele Identifier: CA1726545664

Gene: GNGT1

Linked Data

• dbSNP Id: rs1794418395

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93908937C>A , CM000669.2:g.93908937C>A	GRCh38
NC_000007.13:g.93538249C>A , CM000669.1:g.93538249C>A	GRCh37
NC_000007.12:g.93376185C>A	NCBI36
NG_051196.1:g.7430C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248572.10:c.97-1853C>A MANE Select	ENSP00000248572.5:n.97-1853C>A
ENST00000248572.9:c.97-1853C>A	ENSP00000248572.5:n.97-1853C>A
ENST00000428834.1:c.97-546C>A	ENSP00000401781.1:n.97-546C>A
ENST00000429473.1:c.97-1853C>A	ENSP00000388777.1:n.97-1853C>A
ENST00000430875.1:c.97-546C>A	ENSP00000395756.1:n.97-546C>A
ENST00000455502.5:c.97-546C>A	ENSP00000395857.1:n.97-546C>A
NM_021955.3:c.97-1853C>A	NP_068774.1:n.97-1853C>A
NM_001329426.1:c.97-1853C>A	NP_001316355.1:n.97-1853C>A
NM_021955.4:c.97-1853C>A	NP_068774.1:n.97-1853C>A
NM_001329426.2:c.97-1853C>A	NP_001316355.1:n.97-1853C>A
NM_021955.5:c.97-1853C>A MANE Select	NP_068774.1:n.97-1853C>A