Canonical Allele Identifier: CA1428758859

Gene: CLDN16

Linked Data

• dbSNP Id: rs1719035558

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404346A>T , CM000665.2:g.190404346A>T	GRCh38
NC_000003.11:g.190122135A>T , CM000665.1:g.190122135A>T	GRCh37
NC_000003.10:g.191604829A>T	NCBI36
NG_008149.1:g.21295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-416A>T MANE Select	ENSP00000264734.3:n.218-416A>T
ENST00000456423.2:c.115-5557A>T	ENSP00000414136.2:n.115-5557A>T
ENST00000264734.2:c.428-416A>T	ENSP00000264734.2:n.428-416A>T
ENST00000456423.1:c.325-5557A>T	ENSP00000414136.1:n.325-5557A>T
ENST00000468220.1:n.410-416A>T
NM_006580.3:c.428-416A>T	NP_006571.1:n.428-416A>T
NM_001378492.1:c.218-416A>T	NP_001365421.1:n.218-416A>T
NM_001378493.1:c.218-416A>T	NP_001365422.1:n.218-416A>T
NM_006580.4:c.218-416A>T MANE Select	NP_006571.2:n.218-416A>T