Canonical Allele Identifier: CA2669054087

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190388021-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388022_190388023insTG , CM000665.2:g.190388022_190388023insTG	GRCh38
NC_000003.11:g.190105811_190105812insTG , CM000665.1:g.190105811_190105812insTG	GRCh37
NC_000003.10:g.191588505_191588506insTG	NCBI36
NG_008149.1:g.4971_4972insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-98_-97insTG	ENSP00000264734.2:n.-98_-97insTG
ENST00000468220.1:n.306+13419_306+13420insTG
NM_006580.3:c.-98_-97insTG	NP_006571.1:n.-98_-97insTG
NM_001378492.1:c.-93-215_-93-214insTG	NP_001365421.1:n.-93-215_-93-214insTG
NM_001378493.1:c.-93-215_-93-214insTG	NP_001365422.1:n.-93-215_-93-214insTG