Canonical Allele Identifier: CA1428757103

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402437C= , CM000665.2:g.190402437C=	GRCh38
NC_000003.11:g.190120226C= , CM000665.1:g.190120226C=	GRCh37
NC_000003.10:g.191602920C=	NCBI36
NG_008149.1:g.19386C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.215C= MANE Select	ENSP00000264734.3:p.Pro72=
ENST00000456423.2:c.115-7466C=	ENSP00000414136.2:n.115-7466C=
ENST00000264734.2:c.425C=	ENSP00000264734.2:p.Pro142=
ENST00000456423.1:c.325-7466C=	ENSP00000414136.1:n.325-7466C=
ENST00000468220.1:n.407C=
NM_006580.3:c.425C=	NP_006571.1:p.Pro142=
NM_001378492.1:c.215C=	NP_001365421.1:p.Pro72=
NM_001378493.1:c.215C=	NP_001365422.1:p.Pro72=
NM_006580.4:c.215C= MANE Select	NP_006571.2:p.Pro72=