Canonical Allele Identifier: CA1428757236

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402551C= , CM000665.2:g.190402551C=	GRCh38
NC_000003.11:g.190120340C= , CM000665.1:g.190120340C=	GRCh37
NC_000003.10:g.191603034C=	NCBI36
NG_008149.1:g.19500C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+112C= MANE Select	ENSP00000264734.3:n.217+112C=
ENST00000456423.2:c.115-7352C=	ENSP00000414136.2:n.115-7352C=
ENST00000264734.2:c.427+112C=	ENSP00000264734.2:n.427+112C=
ENST00000456423.1:c.325-7352C=	ENSP00000414136.1:n.325-7352C=
ENST00000468220.1:n.409+112C=
NM_006580.3:c.427+112C=	NP_006571.1:n.427+112C=
NM_001378492.1:c.217+112C=	NP_001365421.1:n.217+112C=
NM_001378493.1:c.217+112C=	NP_001365422.1:n.217+112C=
NM_006580.4:c.217+112C= MANE Select	NP_006571.2:n.217+112C=