Canonical Allele Identifier: CA437637186

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190106037A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388248A>T , CM000665.2:g.190388248A>T	GRCh38
NC_000003.11:g.190106037A>T , CM000665.1:g.190106037A>T	GRCh37
NC_000003.10:g.191588731A>T	NCBI36
NG_008149.1:g.5197A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.-82A>T MANE Select	ENSP00000264734.3:n.-82A>T
ENST00000456423.2:c.-82A>T	ENSP00000414136.2:n.-82A>T
ENST00000264734.2:c.129A>T	ENSP00000264734.2:p.Thr43=
ENST00000456423.1:c.129A>T	ENSP00000414136.1:p.Thr43=
ENST00000468220.1:n.306+13645A>T
NM_006580.3:c.129A>T	NP_006571.1:p.Thr43=
NM_001378492.1:c.-82A>T	NP_001365421.1:n.-82A>T
NM_001378493.1:c.-82A>T	NP_001365422.1:n.-82A>T
NM_006580.4:c.-82A>T MANE Select	NP_006571.2:n.-82A>T