Canonical Allele Identifier: CA801348

Gene: CLDN19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42735970G>A , CM000663.2:g.42735970G>A	GRCh38
NC_000001.10:g.43201641G>A , CM000663.1:g.43201641G>A	GRCh37
NC_000001.9:g.42974228G>A	NCBI36
NG_008993.1:g.9285C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_148960.3:c.534C>T MANE Select	NP_683763.2:p.Gly178=
ENST00000296387.6:c.534C>T MANE Select	ENSP00000296387.1:p.Gly178=
NM_001123395.1:c.534C>T	NP_001116867.1:p.Gly178=
NM_001123395.2:c.534C>T	NP_001116867.1:p.Gly178=
NM_001185117.1:c.449C>T	NP_001172046.1:p.Ala150Val
NM_001185117.2:c.449C>T	NP_001172046.1:p.Ala150Val
NM_148960.2:c.534C>T	NP_683763.2:p.Gly178=
ENST00000296387.5:c.534C>T	ENSP00000296387.1:p.Gly178=
ENST00000372539.3:c.534C>T	ENSP00000361617.3:p.Gly178=
ENST00000539749.5:c.449C>T	ENSP00000443229.1:p.Ala150Val