Canonical Allele Identifier: CA1424460344
Gene: DNAJC19 HGNC NCBI

Linked Data

dbSNP Id: rs1577025126

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180987055T>A , CM000665.2:g.180987055T>A GRCh38
NC_000003.11:g.180704843T>A , CM000665.1:g.180704843T>A GRCh37
NC_000003.10:g.182187537T>A NCBI36
NG_022933.1:g.7720A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.201-33A>T
ENST00000482363.2:n.1264A>T
ENST00000485675.2:n.1258A>T
ENST00000688055.1:c.130-33A>T ENSP00000508688.1:n.130-33A>T
ENST00000382564.8:c.130-33A>T MANE Select ENSP00000372005.2:n.130-33A>T
ENST00000643241.1:c.55-33A>T ENSP00000496401.1:n.55-33A>T
ENST00000646965.1:c.-46-1059A>T ENSP00000496456.1:n.-46-1059A>T
ENST00000382564.6:c.130-33A>T ENSP00000372005.2:n.130-33A>T
ENST00000469657.5:c.129+968A>T ENSP00000418058.1:n.129+968A>T
ENST00000478723.5:n.269-33A>T
ENST00000479269.5:c.55-33A>T ENSP00000419191.1:n.55-33A>T
ENST00000485675.1:n.1170A>T
ENST00000486355.1:c.130-33A>T ENSP00000419991.1:n.130-33A>T
ENST00000491873.5:c.55-33A>T ENSP00000420767.1:n.55-33A>T
NM_001190233.1:c.55-33A>T NP_001177162.1:n.55-33A>T
NM_145261.3:c.130-33A>T NP_660304.1:n.130-33A>T
NR_033721.1:n.250-33A>T
NR_033722.1:n.301+968A>T
NR_033723.1:n.302-33A>T
NR_046073.1:n.176-1059A>T
NM_145261.4:c.130-33A>T MANE Select NP_660304.1:n.130-33A>T
NM_001190233.2:c.55-33A>T NP_001177162.1:n.55-33A>T
NR_033721.2:n.212-33A>T
NR_033722.2:n.263+968A>T