Canonical Allele Identifier: CA1726545723

Gene: GNGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93909011T= , CM000669.2:g.93909011T=	GRCh38
NC_000007.13:g.93538323T= , CM000669.1:g.93538323T=	GRCh37
NC_000007.12:g.93376259T=	NCBI36
NG_051196.1:g.7504T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248572.10:c.97-1779T= MANE Select	ENSP00000248572.5:n.97-1779T=
ENST00000248572.9:c.97-1779T=	ENSP00000248572.5:n.97-1779T=
ENST00000428834.1:c.97-472T=	ENSP00000401781.1:n.97-472T=
ENST00000429473.1:c.97-1779T=	ENSP00000388777.1:n.97-1779T=
ENST00000430875.1:c.97-472T=	ENSP00000395756.1:n.97-472T=
ENST00000455502.5:c.97-472T=	ENSP00000395857.1:n.97-472T=
NM_021955.3:c.97-1779T=	NP_068774.1:n.97-1779T=
NM_001329426.1:c.97-1779T=	NP_001316355.1:n.97-1779T=
NM_021955.4:c.97-1779T=	NP_068774.1:n.97-1779T=
NM_001329426.2:c.97-1779T=	NP_001316355.1:n.97-1779T=
NM_021955.5:c.97-1779T= MANE Select	NP_068774.1:n.97-1779T=