Canonical Allele Identifier: CA843958220

Gene: GNGT1

Linked Data

• dbSNP Id: rs1237099767
• MyVariant Identifiers: chr7:g.93538326C>A (hg19) ; chr7:g.93909014C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93909014C>A , CM000669.2:g.93909014C>A	GRCh38
NC_000007.13:g.93538326C>A , CM000669.1:g.93538326C>A	GRCh37
NC_000007.12:g.93376262C>A	NCBI36
NG_051196.1:g.7507C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248572.10:c.97-1776C>A MANE Select	ENSP00000248572.5:n.97-1776C>A
ENST00000248572.9:c.97-1776C>A	ENSP00000248572.5:n.97-1776C>A
ENST00000428834.1:c.97-469C>A	ENSP00000401781.1:n.97-469C>A
ENST00000429473.1:c.97-1776C>A	ENSP00000388777.1:n.97-1776C>A
ENST00000430875.1:c.97-469C>A	ENSP00000395756.1:n.97-469C>A
ENST00000455502.5:c.97-469C>A	ENSP00000395857.1:n.97-469C>A
NM_021955.3:c.97-1776C>A	NP_068774.1:n.97-1776C>A
NM_001329426.1:c.97-1776C>A	NP_001316355.1:n.97-1776C>A
NM_021955.4:c.97-1776C>A	NP_068774.1:n.97-1776C>A
NM_001329426.2:c.97-1776C>A	NP_001316355.1:n.97-1776C>A
NM_021955.5:c.97-1776C>A MANE Select	NP_068774.1:n.97-1776C>A