Canonical Allele Identifier: CA1428756715

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402155_190402156delinsCA , CM000665.2:g.190402155_190402156delinsCA	GRCh38
NC_000003.11:g.190119944_190119945delinsCA , CM000665.1:g.190119944_190119945delinsCA	GRCh37
NC_000003.10:g.191602638_191602639delinsCA	NCBI36
NG_008149.1:g.19104_19105delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-182_115-181delinsCA MANE Select	ENSP00000264734.3:n.115-182_115-181delinsCA
ENST00000456423.2:c.115-7748_115-7747delinsCA	ENSP00000414136.2:n.115-7748_115-7747delinsCA
ENST00000264734.2:c.325-182_325-181delinsCA	ENSP00000264734.2:n.325-182_325-181delinsCA
ENST00000456423.1:c.325-7748_325-7747delinsCA	ENSP00000414136.1:n.325-7748_325-7747delinsCA
ENST00000468220.1:n.307-182_307-181delinsCA
NM_006580.3:c.325-182_325-181delinsCA	NP_006571.1:n.325-182_325-181delinsCA
NM_001378492.1:c.115-182_115-181delinsCA	NP_001365421.1:n.115-182_115-181delinsCA
NM_001378493.1:c.115-182_115-181delinsCA	NP_001365422.1:n.115-182_115-181delinsCA
NM_006580.4:c.115-182_115-181delinsCA MANE Select	NP_006571.2:n.115-182_115-181delinsCA