Canonical Allele Identifier: CA1057667152

Gene: CLDN16

Linked Data

• dbSNP Id: rs1719044016
• gnomAD v3: 3-190404683-G-GC
• gnomAD v4: 3-190404683-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404683_190404684insC , CM000665.2:g.190404683_190404684insC	GRCh38
NC_000003.11:g.190122472_190122473insC , CM000665.1:g.190122472_190122473insC	GRCh37
NC_000003.10:g.191605166_191605167insC	NCBI36
NG_008149.1:g.21632_21633insC

Transcript Alleles

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