Canonical Allele Identifier: CA903453540

Gene: DNAJC19

Linked Data

• dbSNP Id: rs372386404
• MyVariant Identifiers: chr3:g.180706043T>A (hg19) ; chr3:g.180988255T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180988255T>A , CM000665.2:g.180988255T>A	GRCh38
NC_000003.11:g.180706043T>A , CM000665.1:g.180706043T>A	GRCh37
NC_000003.10:g.182188737T>A	NCBI36
NG_022933.1:g.6520A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478723.6:n.75-26A>T
ENST00000482363.2:n.171-26A>T
ENST00000485675.2:n.165-26A>T
ENST00000688055.1:c.4-26A>T	ENSP00000508688.1:n.4-26A>T
ENST00000382564.8:c.4-26A>T MANE Select	ENSP00000372005.2:n.4-26A>T
ENST00000643241.1:c.-72-26A>T	ENSP00000496401.1:n.-72-26A>T
ENST00000646965.1:c.-47+1345A>T	ENSP00000496456.1:n.-47+1345A>T
ENST00000382564.6:c.4-26A>T	ENSP00000372005.2:n.4-26A>T
ENST00000469657.5:c.4-26A>T	ENSP00000418058.1:n.4-26A>T
ENST00000472504.1:n.176-26A>T
ENST00000478723.5:n.143-26A>T
ENST00000479269.5:c.-72-26A>T	ENSP00000419191.1:n.-72-26A>T
ENST00000482363.1:n.165-26A>T
ENST00000485675.1:n.129-159A>T
ENST00000486355.1:c.4-26A>T	ENSP00000419991.1:n.4-26A>T
ENST00000491873.5:c.-20-159A>T	ENSP00000420767.1:n.-20-159A>T
NM_001190233.1:c.-72-26A>T	NP_001177162.1:n.-72-26A>T
NM_145261.3:c.4-26A>T	NP_660304.1:n.4-26A>T
NR_033721.1:n.176-159A>T
NR_033722.1:n.176-26A>T
NR_033723.1:n.176-26A>T
NR_046073.1:n.175+1345A>T
NM_145261.4:c.4-26A>T MANE Select	NP_660304.1:n.4-26A>T
NM_001190233.2:c.-72-26A>T	NP_001177162.1:n.-72-26A>T
NR_033721.2:n.138-159A>T
NR_033722.2:n.138-26A>T