Canonical Allele Identifier: CA1428758869

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404351_190404353delinsTAA , CM000665.2:g.190404351_190404353delinsTAA	GRCh38
NC_000003.11:g.190122140_190122142delinsTAA , CM000665.1:g.190122140_190122142delinsTAA	GRCh37
NC_000003.10:g.191604834_191604836delinsTAA	NCBI36
NG_008149.1:g.21300_21302delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-411_218-409delinsTAA MANE Select	ENSP00000264734.3:n.218-411_218-409delinsTAA
ENST00000456423.2:c.115-5552_115-5550delinsTAA	ENSP00000414136.2:n.115-5552_115-5550delinsTAA
ENST00000264734.2:c.428-411_428-409delinsTAA	ENSP00000264734.2:n.428-411_428-409delinsTAA
ENST00000456423.1:c.325-5552_325-5550delinsTAA	ENSP00000414136.1:n.325-5552_325-5550delinsTAA
ENST00000468220.1:n.410-411_410-409delinsTAA
NM_006580.3:c.428-411_428-409delinsTAA	NP_006571.1:n.428-411_428-409delinsTAA
NM_001378492.1:c.218-411_218-409delinsTAA	NP_001365421.1:n.218-411_218-409delinsTAA
NM_001378493.1:c.218-411_218-409delinsTAA	NP_001365422.1:n.218-411_218-409delinsTAA
NM_006580.4:c.218-411_218-409delinsTAA MANE Select	NP_006571.2:n.218-411_218-409delinsTAA