Canonical Allele Identifier: CA1428759667

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404964_190404966delinsACT , CM000665.2:g.190404964_190404966delinsACT	GRCh38
NC_000003.11:g.190122753_190122755delinsACT , CM000665.1:g.190122753_190122755delinsACT	GRCh37
NC_000003.10:g.191605447_191605449delinsACT	NCBI36
NG_008149.1:g.21913_21915delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+38_382+40delinsACT MANE Select	ENSP00000264734.3:n.382+38_382+40delinsACT
ENST00000456423.2:c.115-4939_115-4937delinsACT	ENSP00000414136.2:n.115-4939_115-4937delinsACT
ENST00000264734.2:c.592+38_592+40delinsACT	ENSP00000264734.2:n.592+38_592+40delinsACT
ENST00000456423.1:c.325-4939_325-4937delinsACT	ENSP00000414136.1:n.325-4939_325-4937delinsACT
NM_006580.3:c.592+38_592+40delinsACT	NP_006571.1:n.592+38_592+40delinsACT
NM_001378492.1:c.382+38_382+40delinsACT	NP_001365421.1:n.382+38_382+40delinsACT
NM_001378493.1:c.382+38_382+40delinsACT	NP_001365422.1:n.382+38_382+40delinsACT
NM_006580.4:c.382+38_382+40delinsACT MANE Select	NP_006571.2:n.382+38_382+40delinsACT