Canonical Allele Identifier: CA2669041413

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190402580-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402580T>G , CM000665.2:g.190402580T>G	GRCh38
NC_000003.11:g.190120369T>G , CM000665.1:g.190120369T>G	GRCh37
NC_000003.10:g.191603063T>G	NCBI36
NG_008149.1:g.19529T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+141T>G MANE Select	ENSP00000264734.3:n.217+141T>G
ENST00000456423.2:c.115-7323T>G	ENSP00000414136.2:n.115-7323T>G
ENST00000264734.2:c.427+141T>G	ENSP00000264734.2:n.427+141T>G
ENST00000456423.1:c.325-7323T>G	ENSP00000414136.1:n.325-7323T>G
ENST00000468220.1:n.409+141T>G
NM_006580.3:c.427+141T>G	NP_006571.1:n.427+141T>G
NM_001378492.1:c.217+141T>G	NP_001365421.1:n.217+141T>G
NM_001378493.1:c.217+141T>G	NP_001365422.1:n.217+141T>G
NM_006580.4:c.217+141T>G MANE Select	NP_006571.2:n.217+141T>G