Canonical Allele Identifier: CA1428756753

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402198_190402199delinsTG , CM000665.2:g.190402198_190402199delinsTG	GRCh38
NC_000003.11:g.190119987_190119988delinsTG , CM000665.1:g.190119987_190119988delinsTG	GRCh37
NC_000003.10:g.191602681_191602682delinsTG	NCBI36
NG_008149.1:g.19147_19148delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-139_115-138delinsTG MANE Select	ENSP00000264734.3:n.115-139_115-138delinsTG
ENST00000456423.2:c.115-7705_115-7704delinsTG	ENSP00000414136.2:n.115-7705_115-7704delinsTG
ENST00000264734.2:c.325-139_325-138delinsTG	ENSP00000264734.2:n.325-139_325-138delinsTG
ENST00000456423.1:c.325-7705_325-7704delinsTG	ENSP00000414136.1:n.325-7705_325-7704delinsTG
ENST00000468220.1:n.307-139_307-138delinsTG
NM_006580.3:c.325-139_325-138delinsTG	NP_006571.1:n.325-139_325-138delinsTG
NM_001378492.1:c.115-139_115-138delinsTG	NP_001365421.1:n.115-139_115-138delinsTG
NM_001378493.1:c.115-139_115-138delinsTG	NP_001365422.1:n.115-139_115-138delinsTG
NM_006580.4:c.115-139_115-138delinsTG MANE Select	NP_006571.2:n.115-139_115-138delinsTG