Canonical Allele Identifier: CA89760883

Gene: CLDN16

Linked Data

• dbSNP Id: rs34930170
• MyVariant Identifiers: chr3:g.190119877_190119878insA (hg19) ; chr3:g.190402088_190402089insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402088_190402089insA , CM000665.2:g.190402088_190402089insA	GRCh38
NC_000003.11:g.190119877_190119878insA , CM000665.1:g.190119877_190119878insA	GRCh37
NC_000003.10:g.191602571_191602572insA	NCBI36
NG_008149.1:g.19037_19038insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-249_115-248insA MANE Select	ENSP00000264734.3:n.115-249_115-248insA
ENST00000456423.2:c.115-7815_115-7814insA	ENSP00000414136.2:n.115-7815_115-7814insA
ENST00000264734.2:c.325-249_325-248insA	ENSP00000264734.2:n.325-249_325-248insA
ENST00000456423.1:c.325-7815_325-7814insA	ENSP00000414136.1:n.325-7815_325-7814insA
ENST00000468220.1:n.307-249_307-248insA
NM_006580.3:c.325-249_325-248insA	NP_006571.1:n.325-249_325-248insA
NM_001378492.1:c.115-249_115-248insA	NP_001365421.1:n.115-249_115-248insA
NM_001378493.1:c.115-249_115-248insA	NP_001365422.1:n.115-249_115-248insA
NM_006580.4:c.115-249_115-248insA MANE Select	NP_006571.2:n.115-249_115-248insA