Canonical Allele Identifier: CA2717053

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984730dup , CM000665.2:g.180984730dup	GRCh38
NC_000003.11:g.180702518dup , CM000665.1:g.180702518dup	GRCh37
NC_000003.10:g.182185212dup	NCBI36
NG_022933.1:g.10050dup

Transcript Alleles

HGVS	Amino-acid Change
NM_145261.4:c.281-15dup MANE Select	NP_660304.1:n.281-15dup
ENST00000382564.8:c.281-15dup MANE Select	ENSP00000372005.2:n.281-15dup
NM_001190233.1:c.206-15dup	NP_001177162.1:n.206-15dup
NM_001190233.2:c.206-15dup	NP_001177162.1:n.206-15dup
NM_145261.3:c.281-15dup	NP_660304.1:n.281-15dup
NR_033721.1:n.401-15dup
NR_033721.2:n.363-15dup
NR_033722.1:n.373-15dup
NR_033722.2:n.335-15dup
NR_033723.1:n.398-15dup
NR_046073.1:n.247-15dup
ENST00000382564.6:c.281-15dup	ENSP00000372005.2:n.281-15dup
ENST00000469657.5:c.*57-15dup	ENSP00000418058.1:n.*57-15dup
ENST00000479269.5:c.206-15dup	ENSP00000419191.1:n.206-15dup
ENST00000482363.2:n.2394-15dup
ENST00000485675.2:n.3588dup
ENST00000486355.1:c.*46-15dup	ENSP00000419991.1:n.*46-15dup
ENST00000491873.5:c.206-15dup	ENSP00000420767.1:n.206-15dup
ENST00000643241.1:c.*57-15dup	ENSP00000496401.1:n.*57-15dup
ENST00000646965.1:c.26-15dup	ENSP00000496456.1:n.26-15dup
ENST00000688055.1:c.*1193dup	ENSP00000508688.1:n.*1193dup