Canonical Allele Identifier: CA1428759705

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405028_190405029delinsGT , CM000665.2:g.190405028_190405029delinsGT	GRCh38
NC_000003.11:g.190122817_190122818delinsGT , CM000665.1:g.190122817_190122818delinsGT	GRCh37
NC_000003.10:g.191605511_191605512delinsGT	NCBI36
NG_008149.1:g.21977_21978delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+102_382+103delinsGT MANE Select	ENSP00000264734.3:n.382+102_382+103delinsGT
ENST00000456423.2:c.115-4875_115-4874delinsGT	ENSP00000414136.2:n.115-4875_115-4874delinsGT
ENST00000264734.2:c.592+102_592+103delinsGT	ENSP00000264734.2:n.592+102_592+103delinsGT
ENST00000456423.1:c.325-4875_325-4874delinsGT	ENSP00000414136.1:n.325-4875_325-4874delinsGT
NM_006580.3:c.592+102_592+103delinsGT	NP_006571.1:n.592+102_592+103delinsGT
NM_001378492.1:c.382+102_382+103delinsGT	NP_001365421.1:n.382+102_382+103delinsGT
NM_001378493.1:c.382+102_382+103delinsGT	NP_001365422.1:n.382+102_382+103delinsGT
NM_006580.4:c.382+102_382+103delinsGT MANE Select	NP_006571.2:n.382+102_382+103delinsGT