Canonical Allele Identifier: CA2669041498

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190404679-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404679G>C , CM000665.2:g.190404679G>C	GRCh38
NC_000003.11:g.190122468G>C , CM000665.1:g.190122468G>C	GRCh37
NC_000003.10:g.191605162G>C	NCBI36
NG_008149.1:g.21628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-83G>C MANE Select	ENSP00000264734.3:n.218-83G>C
ENST00000456423.2:c.115-5224G>C	ENSP00000414136.2:n.115-5224G>C
ENST00000264734.2:c.428-83G>C	ENSP00000264734.2:n.428-83G>C
ENST00000456423.1:c.325-5224G>C	ENSP00000414136.1:n.325-5224G>C
ENST00000468220.1:n.410-83G>C
NM_006580.3:c.428-83G>C	NP_006571.1:n.428-83G>C
NM_001378492.1:c.218-83G>C	NP_001365421.1:n.218-83G>C
NM_001378493.1:c.218-83G>C	NP_001365422.1:n.218-83G>C
NM_006580.4:c.218-83G>C MANE Select	NP_006571.2:n.218-83G>C