Canonical Allele Identifier: CA2759872224

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408224_190408225insAAAATG , CM000665.2:g.190408224_190408225insAAAATG	GRCh38
NC_000003.11:g.190126013_190126014insAAAATG , CM000665.1:g.190126013_190126014insAAAATG	GRCh37
NC_000003.10:g.191608707_191608708insAAAATG	NCBI36
NG_008149.1:g.25173_25174insAAAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.383-90_383-89insAAAATG MANE Select	ENSP00000264734.3:n.383-90_383-89insAAAATG
ENST00000456423.2:c.115-1679_115-1678insAAAATG	ENSP00000414136.2:n.115-1679_115-1678insAAAATG
ENST00000264734.2:c.593-90_593-89insAAAATG	ENSP00000264734.2:n.593-90_593-89insAAAATG
ENST00000456423.1:c.325-1679_325-1678insAAAATG	ENSP00000414136.1:n.325-1679_325-1678insAAAATG
NM_006580.3:c.593-90_593-89insAAAATG	NP_006571.1:n.593-90_593-89insAAAATG
NM_001378492.1:c.383-90_383-89insAAAATG	NP_001365421.1:n.383-90_383-89insAAAATG
NM_001378493.1:c.383-90_383-89insAAAATG	NP_001365422.1:n.383-90_383-89insAAAATG
NM_006580.4:c.383-90_383-89insAAAATG MANE Select	NP_006571.2:n.383-90_383-89insAAAATG