Canonical Allele Identifier: CA1428759153

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404683_190404684delinsGT , CM000665.2:g.190404683_190404684delinsGT	GRCh38
NC_000003.11:g.190122472_190122473delinsGT , CM000665.1:g.190122472_190122473delinsGT	GRCh37
NC_000003.10:g.191605166_191605167delinsGT	NCBI36
NG_008149.1:g.21632_21633delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-79_218-78delinsGT MANE Select	ENSP00000264734.3:n.218-79_218-78delinsGT
ENST00000456423.2:c.115-5220_115-5219delinsGT	ENSP00000414136.2:n.115-5220_115-5219delinsGT
ENST00000264734.2:c.428-79_428-78delinsGT	ENSP00000264734.2:n.428-79_428-78delinsGT
ENST00000456423.1:c.325-5220_325-5219delinsGT	ENSP00000414136.1:n.325-5220_325-5219delinsGT
ENST00000468220.1:n.410-79_410-78delinsGT
NM_006580.3:c.428-79_428-78delinsGT	NP_006571.1:n.428-79_428-78delinsGT
NM_001378492.1:c.218-79_218-78delinsGT	NP_001365421.1:n.218-79_218-78delinsGT
NM_001378493.1:c.218-79_218-78delinsGT	NP_001365422.1:n.218-79_218-78delinsGT
NM_006580.4:c.218-79_218-78delinsGT MANE Select	NP_006571.2:n.218-79_218-78delinsGT