Canonical Allele Identifier: CA1428762460

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408122_190408123delinsTA , CM000665.2:g.190408122_190408123delinsTA	GRCh38
NC_000003.11:g.190125911_190125912delinsTA , CM000665.1:g.190125911_190125912delinsTA	GRCh37
NC_000003.10:g.191608605_191608606delinsTA	NCBI36
NG_008149.1:g.25071_25072delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.383-192_383-191delinsTA MANE Select	ENSP00000264734.3:n.383-192_383-191delinsTA
ENST00000456423.2:c.115-1781_115-1780delinsTA	ENSP00000414136.2:n.115-1781_115-1780delinsTA
ENST00000264734.2:c.593-192_593-191delinsTA	ENSP00000264734.2:n.593-192_593-191delinsTA
ENST00000456423.1:c.325-1781_325-1780delinsTA	ENSP00000414136.1:n.325-1781_325-1780delinsTA
NM_006580.3:c.593-192_593-191delinsTA	NP_006571.1:n.593-192_593-191delinsTA
NM_001378492.1:c.383-192_383-191delinsTA	NP_001365421.1:n.383-192_383-191delinsTA
NM_001378493.1:c.383-192_383-191delinsTA	NP_001365422.1:n.383-192_383-191delinsTA
NM_006580.4:c.383-192_383-191delinsTA MANE Select	NP_006571.2:n.383-192_383-191delinsTA