Canonical Allele Identifier: CA437637249

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190106088A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388299A>T , CM000665.2:g.190388299A>T	GRCh38
NC_000003.11:g.190106088A>T , CM000665.1:g.190106088A>T	GRCh37
NC_000003.10:g.191588782A>T	NCBI36
NG_008149.1:g.5248A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-31A>T MANE Select	ENSP00000264734.3:n.-31A>T
ENST00000456423.2:c.-31A>T	ENSP00000414136.2:n.-31A>T
ENST00000264734.2:c.180A>T	ENSP00000264734.2:p.Pro60=
ENST00000456423.1:c.180A>T	ENSP00000414136.1:p.Pro60=
ENST00000468220.1:n.306+13696A>T
NM_006580.3:c.180A>T	NP_006571.1:p.Pro60=
NM_001378492.1:c.-31A>T	NP_001365421.1:n.-31A>T
NM_001378493.1:c.-31A>T	NP_001365422.1:n.-31A>T
NM_006580.4:c.-31A>T MANE Select	NP_006571.2:n.-31A>T