Canonical Allele Identifier: CA801347

Gene: CLDN19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42735969C>T , CM000663.2:g.42735969C>T	GRCh38
NC_000001.10:g.43201640C>T , CM000663.1:g.43201640C>T	GRCh37
NC_000001.9:g.42974227C>T	NCBI36
NG_008993.1:g.9286G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_148960.3:c.535G>A MANE Select	NP_683763.2:p.Gly179Ser
ENST00000296387.6:c.535G>A MANE Select	ENSP00000296387.1:p.Gly179Ser
NM_001123395.1:c.535G>A	NP_001116867.1:p.Gly179Ser
NM_001123395.2:c.535G>A	NP_001116867.1:p.Gly179Ser
NM_001185117.1:c.450G>A	NP_001172046.1:p.Ala150=
NM_001185117.2:c.450G>A	NP_001172046.1:p.Ala150=
NM_148960.2:c.535G>A	NP_683763.2:p.Gly179Ser
ENST00000296387.5:c.535G>A	ENSP00000296387.1:p.Gly179Ser
ENST00000372539.3:c.535G>A	ENSP00000361617.3:p.Gly179Ser
ENST00000539749.5:c.450G>A	ENSP00000443229.1:p.Ala150=