Canonical Allele Identifier: CA339947294

Gene: CLDN19

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296387.6:c.169C>T MANE Select	ENSP00000296387.1:p.Gln57Ter
ENST00000296387.5:c.169C>T	ENSP00000296387.1:p.Gln57Ter
ENST00000372539.3:c.169C>T	ENSP00000361617.3:p.Gln57Ter
ENST00000539749.5:c.169C>T	ENSP00000443229.1:p.Gln57Ter
NM_001123395.1:c.169C>T	NP_001116867.1:p.Gln57Ter
NM_001185117.1:c.169C>T	NP_001172046.1:p.Gln57Ter
NM_148960.2:c.169C>T	NP_683763.2:p.Gln57Ter
NM_001123395.2:c.169C>T	NP_001116867.1:p.Gln57Ter
NM_148960.3:c.169C>T MANE Select	NP_683763.2:p.Gln57Ter
NM_001185117.2:c.169C>T	NP_001172046.1:p.Gln57Ter