Canonical Allele Identifier: CA893935
Gene: DNAJC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65392405T>C , CM000663.2:g.65392405T>C GRCh38
NC_000001.10:g.65858088T>C , CM000663.1:g.65858088T>C GRCh37
NC_000001.9:g.65630676T>C NCBI36
NG_033843.1:g.132712T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371069.5:c.1469-26T>C MANE Select ENSP00000360108.4:n.1469-26T>C
ENST00000263441.11:c.1259-26T>C ENSP00000263441.7:n.1259-26T>C
ENST00000371069.4:c.1469-26T>C ENSP00000360108.4:n.1469-26T>C
ENST00000395325.7:c.1298-26T>C ENSP00000378735.3:n.1298-26T>C
ENST00000494710.6:c.1391-26T>C ENSP00000473821.1:n.1391-26T>C
NM_001256864.1:c.1469-26T>C NP_001243793.1:n.1469-26T>C
NM_001256865.1:c.1259-26T>C NP_001243794.1:n.1259-26T>C
NM_014787.3:c.1298-26T>C NP_055602.1:n.1298-26T>C
XM_011542483.1:c.1418-26T>C XP_011540785.1:n.1418-26T>C
XM_011542484.1:c.1391-26T>C XP_011540786.1:n.1391-26T>C
XM_011542485.1:c.1304-26T>C XP_011540787.1:n.1304-26T>C
XM_011542486.1:c.1259-26T>C XP_011540788.1:n.1259-26T>C
XM_011542487.1:c.1259-26T>C XP_011540789.1:n.1259-26T>C
XM_011542488.1:c.1259-26T>C XP_011540790.1:n.1259-26T>C
XM_011542489.1:c.824-26T>C XP_011540791.1:n.824-26T>C
NM_001256864.2:c.1469-26T>C MANE Select NP_001243793.1:n.1469-26T>C
NM_014787.4:c.1298-26T>C NP_055602.1:n.1298-26T>C
NM_001256865.2:c.1259-26T>C NP_001243794.1:n.1259-26T>C