Canonical Allele Identifier: CA355762227

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190105969A>T (hg19) ; chr3:g.190388180A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388180A>T , CM000665.2:g.190388180A>T	GRCh38
NC_000003.11:g.190105969A>T , CM000665.1:g.190105969A>T	GRCh37
NC_000003.10:g.191588663A>T	NCBI36
NG_008149.1:g.5129A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-150A>T MANE Select	ENSP00000264734.3:n.-150A>T
ENST00000456423.2:c.-150A>T	ENSP00000414136.2:n.-150A>T
ENST00000264734.2:c.61A>T	ENSP00000264734.2:p.Arg21Ter
ENST00000456423.1:c.61A>T	ENSP00000414136.1:p.Arg21Ter
ENST00000468220.1:n.306+13577A>T
NM_006580.3:c.61A>T	NP_006571.1:p.Arg21Ter
NM_001378492.1:c.-93-57A>T	NP_001365421.1:n.-93-57A>T
NM_001378493.1:c.-93-57A>T	NP_001365422.1:n.-93-57A>T
NM_006580.4:c.-150A>T MANE Select	NP_006571.2:n.-150A>T