Canonical Allele Identifier: CA437416698

Gene: CLDN1 CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190028026A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190310237A>C , CM000665.2:g.190310237A>C	GRCh38
NC_000003.11:g.190028026A>C , CM000665.1:g.190028026A>C	GRCh37
NC_000003.10:g.191510720A>C	NCBI36
NG_021418.1:g.17210T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295522.4:c.405T>G (CLDN1) MANE Select	ENSP00000295522.3:p.Val135=
ENST00000295522.3:c.405T>G (CLDN1)	ENSP00000295522.3:p.Val135=
ENST00000490800.1:n.364T>G (CLDN1)
NM_021101.4:c.405T>G (CLDN1)	NP_066924.1:p.Val135=
XR_001741069.1:n.203-4656A>C
NM_021101.5:c.405T>G (CLDN1) MANE Select	NP_066924.1:p.Val135=
NM_001378492.1:c.-445-4656A>C (CLDN16)	NP_001365421.1:n.-445-4656A>C
NM_001378493.1:c.-279+19646A>C (CLDN16)	NP_001365422.1:n.-279+19646A>C