Canonical Allele Identifier: CA355762580

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190106139C>A (hg19) ; chr3:g.190388350C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388350C>A , CM000665.2:g.190388350C>A	GRCh38
NC_000003.11:g.190106139C>A , CM000665.1:g.190106139C>A	GRCh37
NC_000003.10:g.191588833C>A	NCBI36
NG_008149.1:g.5299C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.21C>A MANE Select	ENSP00000264734.3:p.Tyr7Ter
ENST00000456423.2:c.21C>A	ENSP00000414136.2:p.Tyr7Ter
ENST00000264734.2:c.231C>A	ENSP00000264734.2:p.Tyr77Ter
ENST00000456423.1:c.231C>A	ENSP00000414136.1:p.Tyr77Ter
ENST00000468220.1:n.306+13747C>A
NM_006580.3:c.231C>A	NP_006571.1:p.Tyr77Ter
NM_001378492.1:c.21C>A	NP_001365421.1:p.Tyr7Ter
NM_001378493.1:c.21C>A	NP_001365422.1:p.Tyr7Ter
NM_006580.4:c.21C>A MANE Select	NP_006571.2:p.Tyr7Ter