Canonical Allele Identifier: CA1428757340

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402640_190402641delinsTA , CM000665.2:g.190402640_190402641delinsTA	GRCh38
NC_000003.11:g.190120429_190120430delinsTA , CM000665.1:g.190120429_190120430delinsTA	GRCh37
NC_000003.10:g.191603123_191603124delinsTA	NCBI36
NG_008149.1:g.19589_19590delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+201_217+202delinsTA MANE Select	ENSP00000264734.3:n.217+201_217+202delinsTA
ENST00000456423.2:c.115-7263_115-7262delinsTA	ENSP00000414136.2:n.115-7263_115-7262delinsTA
ENST00000264734.2:c.427+201_427+202delinsTA	ENSP00000264734.2:n.427+201_427+202delinsTA
ENST00000456423.1:c.325-7263_325-7262delinsTA	ENSP00000414136.1:n.325-7263_325-7262delinsTA
ENST00000468220.1:n.409+201_409+202delinsTA
NM_006580.3:c.427+201_427+202delinsTA	NP_006571.1:n.427+201_427+202delinsTA
NM_001378492.1:c.217+201_217+202delinsTA	NP_001365421.1:n.217+201_217+202delinsTA
NM_001378493.1:c.217+201_217+202delinsTA	NP_001365422.1:n.217+201_217+202delinsTA
NM_006580.4:c.217+201_217+202delinsTA MANE Select	NP_006571.2:n.217+201_217+202delinsTA