Canonical Allele Identifier: CA1428758878

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404358_190404362delinsATTAT , CM000665.2:g.190404358_190404362delinsATTAT	GRCh38
NC_000003.11:g.190122147_190122151delinsATTAT , CM000665.1:g.190122147_190122151delinsATTAT	GRCh37
NC_000003.10:g.191604841_191604845delinsATTAT	NCBI36
NG_008149.1:g.21307_21311delinsATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-404_218-400delinsATTAT MANE Select	ENSP00000264734.3:n.218-404_218-400delinsATTAT
ENST00000456423.2:c.115-5545_115-5541delinsATTAT	ENSP00000414136.2:n.115-5545_115-5541delinsATTAT
ENST00000264734.2:c.428-404_428-400delinsATTAT	ENSP00000264734.2:n.428-404_428-400delinsATTAT
ENST00000456423.1:c.325-5545_325-5541delinsATTAT	ENSP00000414136.1:n.325-5545_325-5541delinsATTAT
ENST00000468220.1:n.410-404_410-400delinsATTAT
NM_006580.3:c.428-404_428-400delinsATTAT	NP_006571.1:n.428-404_428-400delinsATTAT
NM_001378492.1:c.218-404_218-400delinsATTAT	NP_001365421.1:n.218-404_218-400delinsATTAT
NM_001378493.1:c.218-404_218-400delinsATTAT	NP_001365422.1:n.218-404_218-400delinsATTAT
NM_006580.4:c.218-404_218-400delinsATTAT MANE Select	NP_006571.2:n.218-404_218-400delinsATTAT