Canonical Allele Identifier: CA1428759662

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404957_190404972delinsTAGGGAGACTCTGCTA , CM000665.2:g.190404957_190404972delinsTAGGGAGACTCTGCTA	GRCh38
NC_000003.11:g.190122746_190122761delinsTAGGGAGACTCTGCTA , CM000665.1:g.190122746_190122761delinsTAGGGAGACTCTGCTA	GRCh37
NC_000003.10:g.191605440_191605455delinsTAGGGAGACTCTGCTA	NCBI36
NG_008149.1:g.21906_21921delinsTAGGGAGACTCTGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+31_382+46delinsTAGGGAGACTCTGCTA MANE Select	ENSP00000264734.3:n.382+31_382+46delinsTAGGGAGACTCTGCTA
ENST00000456423.2:c.115-4946_115-4931delinsTAGGGAGACTCTGCTA	ENSP00000414136.2:n.115-4946_115-4931delinsTAGGGAGACTCTGCTA
ENST00000264734.2:c.592+31_592+46delinsTAGGGAGACTCTGCTA	ENSP00000264734.2:n.592+31_592+46delinsTAGGGAGACTCTGCTA
ENST00000456423.1:c.325-4946_325-4931delinsTAGGGAGACTCTGCTA	ENSP00000414136.1:n.325-4946_325-4931delinsTAGGGAGACTCTGCTA
NM_006580.3:c.592+31_592+46delinsTAGGGAGACTCTGCTA	NP_006571.1:n.592+31_592+46delinsTAGGGAGACTCTGCTA
NM_001378492.1:c.382+31_382+46delinsTAGGGAGACTCTGCTA	NP_001365421.1:n.382+31_382+46delinsTAGGGAGACTCTGCTA
NM_001378493.1:c.382+31_382+46delinsTAGGGAGACTCTGCTA	NP_001365422.1:n.382+31_382+46delinsTAGGGAGACTCTGCTA
NM_006580.4:c.382+31_382+46delinsTAGGGAGACTCTGCTA MANE Select	NP_006571.2:n.382+31_382+46delinsTAGGGAGACTCTGCTA