Canonical Allele Identifier: CA10840088

Gene: DNAJC6

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65316975T>A , CM000663.2:g.65316975T>A	GRCh38
NC_000001.10:g.65782658T>A , CM000663.1:g.65782658T>A	GRCh37
NC_000001.9:g.65555246T>A	NCBI36
NG_033843.1:g.57282T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371069.5:c.193+7037T>A MANE Select	ENSP00000360108.4:n.193+7037T>A
ENST00000263441.11:c.-130-28636T>A	ENSP00000263441.7:n.-130-28636T>A
ENST00000371069.4:c.193+7037T>A	ENSP00000360108.4:n.193+7037T>A
ENST00000395325.7:c.23-47660T>A	ENSP00000378735.3:n.23-47660T>A
ENST00000463018.5:n.86-28636T>A
ENST00000483402.1:n.170-28636T>A
ENST00000494710.6:c.116-47660T>A	ENSP00000473821.1:n.116-47660T>A
NM_001256864.1:c.193+7037T>A	NP_001243793.1:n.193+7037T>A
NM_001256865.1:c.-130-28636T>A	NP_001243794.1:n.-130-28636T>A
NM_014787.3:c.23-47660T>A	NP_055602.1:n.23-47660T>A
XM_011542483.1:c.142+7037T>A	XP_011540785.1:n.142+7037T>A
XM_011542484.1:c.116-47660T>A	XP_011540786.1:n.116-47660T>A
XM_011542485.1:c.29-47660T>A	XP_011540787.1:n.29-47660T>A
XM_011542486.1:c.-130-28636T>A	XP_011540788.1:n.-130-28636T>A
XM_011542487.1:c.-130-28636T>A	XP_011540789.1:n.-130-28636T>A
XM_011542488.1:c.-130-28636T>A	XP_011540790.1:n.-130-28636T>A
XR_002958317.1:n.1429+827T>A
NM_001256864.2:c.193+7037T>A MANE Select	NP_001243793.1:n.193+7037T>A
NM_014787.4:c.23-47660T>A	NP_055602.1:n.23-47660T>A
NM_001256865.2:c.-130-28636T>A	NP_001243794.1:n.-130-28636T>A