Canonical Allele Identifier: CA339947295

Gene: CLDN19

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296387.6:c.169C>A MANE Select	ENSP00000296387.1:p.Gln57Lys
ENST00000296387.5:c.169C>A	ENSP00000296387.1:p.Gln57Lys
ENST00000372539.3:c.169C>A	ENSP00000361617.3:p.Gln57Lys
ENST00000539749.5:c.169C>A	ENSP00000443229.1:p.Gln57Lys
NM_001123395.1:c.169C>A	NP_001116867.1:p.Gln57Lys
NM_001185117.1:c.169C>A	NP_001172046.1:p.Gln57Lys
NM_148960.2:c.169C>A	NP_683763.2:p.Gln57Lys
NM_001123395.2:c.169C>A	NP_001116867.1:p.Gln57Lys
NM_148960.3:c.169C>A MANE Select	NP_683763.2:p.Gln57Lys
NM_001185117.2:c.169C>A	NP_001172046.1:p.Gln57Lys