Canonical Allele Identifier: CA355762245

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190388189-C-T
• MyVariant Identifiers: chr3:g.190105978C>T (hg19) ; chr3:g.190388189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388189C>T , CM000665.2:g.190388189C>T	GRCh38
NC_000003.11:g.190105978C>T , CM000665.1:g.190105978C>T	GRCh37
NC_000003.10:g.191588672C>T	NCBI36
NG_008149.1:g.5138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-141C>T MANE Select	ENSP00000264734.3:n.-141C>T
ENST00000456423.2:c.-141C>T	ENSP00000414136.2:n.-141C>T
ENST00000264734.2:c.70C>T	ENSP00000264734.2:p.Gln24Ter
ENST00000456423.1:c.70C>T	ENSP00000414136.1:p.Gln24Ter
ENST00000468220.1:n.306+13586C>T
NM_006580.3:c.70C>T	NP_006571.1:p.Gln24Ter
NM_001378492.1:c.-93-48C>T	NP_001365421.1:n.-93-48C>T
NM_001378493.1:c.-93-48C>T	NP_001365422.1:n.-93-48C>T
NM_006580.4:c.-141C>T MANE Select	NP_006571.2:n.-141C>T