Canonical Allele Identifier: CA2759870012

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405026A>G , CM000665.2:g.190405026A>G	GRCh38
NC_000003.11:g.190122815A>G , CM000665.1:g.190122815A>G	GRCh37
NC_000003.10:g.191605509A>G	NCBI36
NG_008149.1:g.21975A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+100A>G MANE Select	ENSP00000264734.3:n.382+100A>G
ENST00000456423.2:c.115-4877A>G	ENSP00000414136.2:n.115-4877A>G
ENST00000264734.2:c.592+100A>G	ENSP00000264734.2:n.592+100A>G
ENST00000456423.1:c.325-4877A>G	ENSP00000414136.1:n.325-4877A>G
NM_006580.3:c.592+100A>G	NP_006571.1:n.592+100A>G
NM_001378492.1:c.382+100A>G	NP_001365421.1:n.382+100A>G
NM_001378493.1:c.382+100A>G	NP_001365422.1:n.382+100A>G
NM_006580.4:c.382+100A>G MANE Select	NP_006571.2:n.382+100A>G