Canonical Allele Identifier: CA355766958

Gene: CLDN16

Linked Data

• COSMIC: COSM6297428
• MyVariant Identifiers: chr3:g.190126126G>T (hg19) ; chr3:g.190408337G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408337G>T , CM000665.2:g.190408337G>T	GRCh38
NC_000003.11:g.190126126G>T , CM000665.1:g.190126126G>T	GRCh37
NC_000003.10:g.191608820G>T	NCBI36
NG_008149.1:g.25286G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.406G>T MANE Select	ENSP00000264734.3:p.Val136Leu
ENST00000456423.2:c.115-1566G>T	ENSP00000414136.2:n.115-1566G>T
ENST00000264734.2:c.616G>T	ENSP00000264734.2:p.Val206Leu
ENST00000456423.1:c.325-1566G>T	ENSP00000414136.1:n.325-1566G>T
NM_006580.3:c.616G>T	NP_006571.1:p.Val206Leu
NM_001378492.1:c.406G>T	NP_001365421.1:p.Val136Leu
NM_001378493.1:c.406G>T	NP_001365422.1:p.Val136Leu
NM_006580.4:c.406G>T MANE Select	NP_006571.2:p.Val136Leu