Canonical Allele Identifier: CA339947933

Gene: CLDN19

Linked Data

• MyVariant Identifiers: chr1:g.43205696C>G (hg19) ; chr1:g.42740025C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42740025C>G , CM000663.2:g.42740025C>G	GRCh38
NC_000001.10:g.43205696C>G , CM000663.1:g.43205696C>G	GRCh37
NC_000001.9:g.42978283C>G	NCBI36
NG_008993.1:g.5230G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296387.6:c.39G>C MANE Select	ENSP00000296387.1:p.Leu13Phe
ENST00000296387.5:c.39G>C	ENSP00000296387.1:p.Leu13Phe
ENST00000372539.3:c.39G>C	ENSP00000361617.3:p.Leu13Phe
ENST00000539749.5:c.39G>C	ENSP00000443229.1:p.Leu13Phe
NM_001123395.1:c.39G>C	NP_001116867.1:p.Leu13Phe
NM_001185117.1:c.39G>C	NP_001172046.1:p.Leu13Phe
NM_148960.2:c.39G>C	NP_683763.2:p.Leu13Phe
NM_001123395.2:c.39G>C	NP_001116867.1:p.Leu13Phe
NM_148960.3:c.39G>C MANE Select	NP_683763.2:p.Leu13Phe
NM_001185117.2:c.39G>C	NP_001172046.1:p.Leu13Phe