Canonical Allele Identifier: CA1141579750

Gene: CLDN19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42738540A= , CM000663.2:g.42738540A=	GRCh38
NC_000001.10:g.43204211A= , CM000663.1:g.43204211A=	GRCh37
NC_000001.9:g.42976798A=	NCBI36
NG_008993.1:g.6715T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296387.6:c.269T= MANE Select	ENSP00000296387.1:p.Leu90=
ENST00000296387.5:c.269T=	ENSP00000296387.1:p.Leu90=
ENST00000372539.3:c.269T=	ENSP00000361617.3:p.Leu90=
ENST00000539749.5:c.269T=	ENSP00000443229.1:p.Leu90=
NM_001123395.1:c.269T=	NP_001116867.1:p.Leu90=
NM_001185117.1:c.269T=	NP_001172046.1:p.Leu90=
NM_148960.2:c.269T=	NP_683763.2:p.Leu90=
NM_001123395.2:c.269T=	NP_001116867.1:p.Leu90=
NM_148960.3:c.269T= MANE Select	NP_683763.2:p.Leu90=
NM_001185117.2:c.269T=	NP_001172046.1:p.Leu90=