Canonical Allele Identifier: CA339947812

Gene: CLDN19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42740005C>A , CM000663.2:g.42740005C>A	GRCh38
NC_000001.10:g.43205676C>A , CM000663.1:g.43205676C>A	GRCh37
NC_000001.9:g.42978263C>A	NCBI36
NG_008993.1:g.5250G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_148960.3:c.59G>T MANE Select	NP_683763.2:p.Gly20Val
ENST00000296387.6:c.59G>T MANE Select	ENSP00000296387.1:p.Gly20Val
NM_001123395.1:c.59G>T	NP_001116867.1:p.Gly20Val
NM_001123395.2:c.59G>T	NP_001116867.1:p.Gly20Val
NM_001185117.1:c.59G>T	NP_001172046.1:p.Gly20Val
NM_001185117.2:c.59G>T	NP_001172046.1:p.Gly20Val
NM_148960.2:c.59G>T	NP_683763.2:p.Gly20Val
ENST00000296387.5:c.59G>T	ENSP00000296387.1:p.Gly20Val
ENST00000372539.3:c.59G>T	ENSP00000361617.3:p.Gly20Val
ENST00000539749.5:c.59G>T	ENSP00000443229.1:p.Gly20Val