Canonical Allele Identifier: CA355766035

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190122590A>T (hg19) ; chr3:g.190404801A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404801A>T , CM000665.2:g.190404801A>T	GRCh38
NC_000003.11:g.190122590A>T , CM000665.1:g.190122590A>T	GRCh37
NC_000003.10:g.191605284A>T	NCBI36
NG_008149.1:g.21750A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.257A>T MANE Select	ENSP00000264734.3:p.Asp86Val
ENST00000456423.2:c.115-5102A>T	ENSP00000414136.2:n.115-5102A>T
ENST00000264734.2:c.467A>T	ENSP00000264734.2:p.Asp156Val
ENST00000456423.1:c.325-5102A>T	ENSP00000414136.1:n.325-5102A>T
ENST00000468220.1:n.449A>T
NM_006580.3:c.467A>T	NP_006571.1:p.Asp156Val
NM_001378492.1:c.257A>T	NP_001365421.1:p.Asp86Val
NM_001378493.1:c.257A>T	NP_001365422.1:p.Asp86Val
NM_006580.4:c.257A>T MANE Select	NP_006571.2:p.Asp86Val