Canonical Allele Identifier: CA355765727

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190120202A>G (hg19) ; chr3:g.190402413A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402413A>G , CM000665.2:g.190402413A>G	GRCh38
NC_000003.11:g.190120202A>G , CM000665.1:g.190120202A>G	GRCh37
NC_000003.10:g.191602896A>G	NCBI36
NG_008149.1:g.19362A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.191A>G MANE Select	ENSP00000264734.3:p.Tyr64Cys
ENST00000456423.2:c.115-7490A>G	ENSP00000414136.2:n.115-7490A>G
ENST00000264734.2:c.401A>G	ENSP00000264734.2:p.Tyr134Cys
ENST00000456423.1:c.325-7490A>G	ENSP00000414136.1:n.325-7490A>G
ENST00000468220.1:n.383A>G
NM_006580.3:c.401A>G	NP_006571.1:p.Tyr134Cys
NM_001378492.1:c.191A>G	NP_001365421.1:p.Tyr64Cys
NM_001378493.1:c.191A>G	NP_001365422.1:p.Tyr64Cys
NM_006580.4:c.191A>G MANE Select	NP_006571.2:p.Tyr64Cys