Canonical Allele Identifier: CA1428735422

Gene: CLDN1 CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190310218T= , CM000665.2:g.190310218T=	GRCh38
NC_000003.11:g.190028007T= , CM000665.1:g.190028007T=	GRCh37
NC_000003.10:g.191510701T=	NCBI36
NG_021418.1:g.17229A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295522.4:c.424A= (CLDN1) MANE Select	ENSP00000295522.3:p.Asn142=
ENST00000295522.3:c.424A= (CLDN1)	ENSP00000295522.3:p.Asn142=
ENST00000490800.1:n.383A= (CLDN1)
NM_021101.4:c.424A= (CLDN1)	NP_066924.1:p.Asn142=
XR_001741069.1:n.203-4675T=
NM_021101.5:c.424A= (CLDN1) MANE Select	NP_066924.1:p.Asn142=
NM_001378492.1:c.-445-4675T= (CLDN16)	NP_001365421.1:n.-445-4675T=
NM_001378493.1:c.-279+19627T= (CLDN16)	NP_001365422.1:n.-279+19627T=