Canonical Allele Identifier: CA1428776006

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388358_190388361delinsGCTT , CM000665.2:g.190388358_190388361delinsGCTT	GRCh38
NC_000003.11:g.190106147_190106150delinsGCTT , CM000665.1:g.190106147_190106150delinsGCTT	GRCh37
NC_000003.10:g.191588841_191588844delinsGCTT	NCBI36
NG_008149.1:g.5307_5310delinsGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.29_32delinsGCTT MANE Select	ENSP00000264734.3:p.Cys10=
ENST00000456423.2:c.29_32delinsGCTT	ENSP00000414136.2:p.Cys10=
ENST00000264734.2:c.239_242delinsGCTT	ENSP00000264734.2:p.Cys80=
ENST00000456423.1:c.239_242delinsGCTT	ENSP00000414136.1:p.Cys80=
ENST00000468220.1:n.306+13755_306+13758delinsGCTT
NM_006580.3:c.239_242delinsGCTT	NP_006571.1:p.Cys80=
NM_001378492.1:c.29_32delinsGCTT	NP_001365421.1:p.Cys10=
NM_001378493.1:c.29_32delinsGCTT	NP_001365422.1:p.Cys10=
NM_006580.4:c.29_32delinsGCTT MANE Select	NP_006571.2:p.Cys10=