Canonical Allele Identifier: CA2669040844

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190402310-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402314_190402315del , CM000665.2:g.190402314_190402315del	GRCh38
NC_000003.11:g.190120103_190120104del , CM000665.1:g.190120103_190120104del	GRCh37
NC_000003.10:g.191602797_191602798del	NCBI36
NG_008149.1:g.19263_19264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-23_115-22del MANE Select	ENSP00000264734.3:n.115-23_115-22del
ENST00000456423.2:c.115-7589_115-7588del	ENSP00000414136.2:n.115-7589_115-7588del
ENST00000264734.2:c.325-23_325-22del	ENSP00000264734.2:n.325-23_325-22del
ENST00000456423.1:c.325-7589_325-7588del	ENSP00000414136.1:n.325-7589_325-7588del
ENST00000468220.1:n.307-23_307-22del
NM_006580.3:c.325-23_325-22del	NP_006571.1:n.325-23_325-22del
NM_001378492.1:c.115-23_115-22del	NP_001365421.1:n.115-23_115-22del
NM_001378493.1:c.115-23_115-22del	NP_001365422.1:n.115-23_115-22del
NM_006580.4:c.115-23_115-22del MANE Select	NP_006571.2:n.115-23_115-22del