Canonical Allele Identifier: CA355766031

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190404800-G-C
• MyVariant Identifiers: chr3:g.190122589G>C (hg19) ; chr3:g.190404800G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404800G>C , CM000665.2:g.190404800G>C	GRCh38
NC_000003.11:g.190122589G>C , CM000665.1:g.190122589G>C	GRCh37
NC_000003.10:g.191605283G>C	NCBI36
NG_008149.1:g.21749G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.256G>C MANE Select	ENSP00000264734.3:p.Asp86His
ENST00000456423.2:c.115-5103G>C	ENSP00000414136.2:n.115-5103G>C
ENST00000264734.2:c.466G>C	ENSP00000264734.2:p.Asp156His
ENST00000456423.1:c.325-5103G>C	ENSP00000414136.1:n.325-5103G>C
ENST00000468220.1:n.448G>C
NM_006580.3:c.466G>C	NP_006571.1:p.Asp156His
NM_001378492.1:c.256G>C	NP_001365421.1:p.Asp86His
NM_001378493.1:c.256G>C	NP_001365422.1:p.Asp86His
NM_006580.4:c.256G>C MANE Select	NP_006571.2:p.Asp86His