Canonical Allele Identifier: CA1141579751
Gene: CLDN19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42739895G= , CM000663.2:g.42739895G= GRCh38
NC_000001.10:g.43205566G= , CM000663.1:g.43205566G= GRCh37
NC_000001.9:g.42978153G= NCBI36
NG_008993.1:g.5360C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296387.6:c.169C= MANE Select ENSP00000296387.1:p.Gln57=
ENST00000296387.5:c.169C= ENSP00000296387.1:p.Gln57=
ENST00000372539.3:c.169C= ENSP00000361617.3:p.Gln57=
ENST00000539749.5:c.169C= ENSP00000443229.1:p.Gln57=
NM_001123395.1:c.169C= NP_001116867.1:p.Gln57=
NM_001185117.1:c.169C= NP_001172046.1:p.Gln57=
NM_148960.2:c.169C= NP_683763.2:p.Gln57=
NM_001123395.2:c.169C= NP_001116867.1:p.Gln57=
NM_148960.3:c.169C= MANE Select NP_683763.2:p.Gln57=
NM_001185117.2:c.169C= NP_001172046.1:p.Gln57=