Canonical Allele Identifier: CA1424460288

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986928_180986932delinsTAGAG , CM000665.2:g.180986928_180986932delinsTAGAG	GRCh38
NC_000003.11:g.180704716_180704720delinsTAGAG , CM000665.1:g.180704716_180704720delinsTAGAG	GRCh37
NC_000003.10:g.182187410_182187414delinsTAGAG	NCBI36
NG_022933.1:g.7843_7847delinsCTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280+11_280+15delinsCTCTA
ENST00000482363.2:n.1387_1391delinsCTCTA
ENST00000485675.2:n.1381_1385delinsCTCTA
ENST00000688055.1:c.209+11_209+15delinsCTCTA	ENSP00000508688.1:n.209+11_209+15delinsCTCTA
ENST00000382564.8:c.209+11_209+15delinsCTCTA MANE Select	ENSP00000372005.2:n.209+11_209+15delinsCTCTA
ENST00000643241.1:c.129+16_129+20delinsCTCTA	ENSP00000496401.1:n.129+16_129+20delinsCTCTA
ENST00000646965.1:c.-46-936_-46-932delinsCTCTA	ENSP00000496456.1:n.-46-936_-46-932delinsCTCTA
ENST00000382564.6:c.209+11_209+15delinsCTCTA	ENSP00000372005.2:n.209+11_209+15delinsCTCTA
ENST00000469657.5:c.130-936_130-932delinsCTCTA	ENSP00000418058.1:n.130-936_130-932delinsCTCTA
ENST00000478723.5:n.348+11_348+15delinsCTCTA
ENST00000479269.5:c.134+11_134+15delinsCTCTA	ENSP00000419191.1:n.134+11_134+15delinsCTCTA
ENST00000485675.1:n.1293_1297delinsCTCTA
ENST00000486355.1:c.154+66_154+70delinsCTCTA	ENSP00000419991.1:n.154+66_154+70delinsCTCTA
ENST00000491873.5:c.134+11_134+15delinsCTCTA	ENSP00000420767.1:n.134+11_134+15delinsCTCTA
NM_001190233.1:c.134+11_134+15delinsCTCTA	NP_001177162.1:n.134+11_134+15delinsCTCTA
NM_145261.3:c.209+11_209+15delinsCTCTA	NP_660304.1:n.209+11_209+15delinsCTCTA
NR_033721.1:n.329+11_329+15delinsCTCTA
NR_033722.1:n.302-936_302-932delinsCTCTA
NR_033723.1:n.326+66_326+70delinsCTCTA
NR_046073.1:n.176-936_176-932delinsCTCTA
NM_145261.4:c.209+11_209+15delinsCTCTA MANE Select	NP_660304.1:n.209+11_209+15delinsCTCTA
NM_001190233.2:c.134+11_134+15delinsCTCTA	NP_001177162.1:n.134+11_134+15delinsCTCTA
NR_033721.2:n.291+11_291+15delinsCTCTA
NR_033722.2:n.264-936_264-932delinsCTCTA