Canonical Allele Identifier: CA355762369

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190106035A>T (hg19) ; chr3:g.190388246A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388246A>T , CM000665.2:g.190388246A>T	GRCh38
NC_000003.11:g.190106035A>T , CM000665.1:g.190106035A>T	GRCh37
NC_000003.10:g.191588729A>T	NCBI36
NG_008149.1:g.5195A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.-84A>T MANE Select	ENSP00000264734.3:n.-84A>T
ENST00000456423.2:c.-84A>T	ENSP00000414136.2:n.-84A>T
ENST00000264734.2:c.127A>T	ENSP00000264734.2:p.Thr43Ser
ENST00000456423.1:c.127A>T	ENSP00000414136.1:p.Thr43Ser
ENST00000468220.1:n.306+13643A>T
NM_006580.3:c.127A>T	NP_006571.1:p.Thr43Ser
NM_001378492.1:c.-84A>T	NP_001365421.1:n.-84A>T
NM_001378493.1:c.-84A>T	NP_001365422.1:n.-84A>T
NM_006580.4:c.-84A>T MANE Select	NP_006571.2:n.-84A>T