Canonical Allele Identifier: CA1428756643

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402104_190402105delinsAC , CM000665.2:g.190402104_190402105delinsAC	GRCh38
NC_000003.11:g.190119893_190119894delinsAC , CM000665.1:g.190119893_190119894delinsAC	GRCh37
NC_000003.10:g.191602587_191602588delinsAC	NCBI36
NG_008149.1:g.19053_19054delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-233_115-232delinsAC MANE Select	ENSP00000264734.3:n.115-233_115-232delinsAC
ENST00000456423.2:c.115-7799_115-7798delinsAC	ENSP00000414136.2:n.115-7799_115-7798delinsAC
ENST00000264734.2:c.325-233_325-232delinsAC	ENSP00000264734.2:n.325-233_325-232delinsAC
ENST00000456423.1:c.325-7799_325-7798delinsAC	ENSP00000414136.1:n.325-7799_325-7798delinsAC
ENST00000468220.1:n.307-233_307-232delinsAC
NM_006580.3:c.325-233_325-232delinsAC	NP_006571.1:n.325-233_325-232delinsAC
NM_001378492.1:c.115-233_115-232delinsAC	NP_001365421.1:n.115-233_115-232delinsAC
NM_001378493.1:c.115-233_115-232delinsAC	NP_001365422.1:n.115-233_115-232delinsAC
NM_006580.4:c.115-233_115-232delinsAC MANE Select	NP_006571.2:n.115-233_115-232delinsAC