Canonical Allele Identifier: CA388484206

Gene: CLDN10

Linked Data

• dbSNP Id: rs387907413
• gnomAD v4: 13-95560419-C-G
• MyVariant Identifiers: chr13:g.96212673C>G (hg19) ; chr13:g.95560419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95560419C>G , CM000675.2:g.95560419C>G	GRCh38
NC_000013.10:g.96212673C>G , CM000675.1:g.96212673C>G	GRCh37
NC_000013.9:g.95010674C>G	NCBI36
NG_047100.1:g.131821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299339.3:c.420C>G MANE Select	ENSP00000299339.2:p.Asn140Lys
ENST00000299339.2:c.420C>G	ENSP00000299339.2:p.Asn140Lys
ENST00000376855.1:c.174C>G	ENSP00000366051.1:p.Asn58Lys
ENST00000376873.7:c.414C>G	ENSP00000366069.2:p.Asn138Lys
NM_001160100.1:c.357C>G	NP_001153572.1:p.Asn119Lys
NM_006984.4:c.420C>G	NP_008915.1:p.Asn140Lys
NM_182848.3:c.414C>G	NP_878268.1:p.Asn138Lys
XM_011521134.1:c.510C>G	XP_011519436.1:p.Asn170Lys
XM_011521134.2:c.510C>G	XP_011519436.1:p.Asn170Lys
XM_017020843.1:c.540C>G	XP_016876332.1:p.Asn180Lys
XM_017020844.1:c.504C>G	XP_016876333.1:p.Asn168Lys
XM_024449432.1:c.174C>G	XP_024305200.1:p.Asn58Lys
NM_006984.5:c.420C>G MANE Select	NP_008915.1:p.Asn140Lys
NM_001160100.2:c.357C>G	NP_001153572.1:p.Asn119Lys
NM_182848.4:c.414C>G	NP_878268.1:p.Asn138Lys