Canonical Allele Identifier: CA23927866
Gene: DNAJC6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65335879C>A , CM000663.2:g.65335879C>A GRCh38
NC_000001.10:g.65801562C>A , CM000663.1:g.65801562C>A GRCh37
NC_000001.9:g.65574150C>A NCBI36
NG_033843.1:g.76186C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371069.5:c.193+25941C>A MANE Select ENSP00000360108.4:n.193+25941C>A
ENST00000263441.11:c.-130-9732C>A ENSP00000263441.7:n.-130-9732C>A
ENST00000371069.4:c.193+25941C>A ENSP00000360108.4:n.193+25941C>A
ENST00000395325.7:c.23-28756C>A ENSP00000378735.3:n.23-28756C>A
ENST00000463018.5:n.86-9732C>A
ENST00000483402.1:n.170-9732C>A
ENST00000494710.6:c.116-28756C>A ENSP00000473821.1:n.116-28756C>A
NM_001256864.1:c.193+25941C>A NP_001243793.1:n.193+25941C>A
NM_001256865.1:c.-130-9732C>A NP_001243794.1:n.-130-9732C>A
NM_014787.3:c.23-28756C>A NP_055602.1:n.23-28756C>A
XM_011542483.1:c.142+25941C>A XP_011540785.1:n.142+25941C>A
XM_011542484.1:c.116-28756C>A XP_011540786.1:n.116-28756C>A
XM_011542485.1:c.29-28756C>A XP_011540787.1:n.29-28756C>A
XM_011542486.1:c.-130-9732C>A XP_011540788.1:n.-130-9732C>A
XM_011542487.1:c.-130-9732C>A XP_011540789.1:n.-130-9732C>A
XM_011542488.1:c.-130-9732C>A XP_011540790.1:n.-130-9732C>A
NM_001256864.2:c.193+25941C>A MANE Select NP_001243793.1:n.193+25941C>A
NM_014787.4:c.23-28756C>A NP_055602.1:n.23-28756C>A
NM_001256865.2:c.-130-9732C>A NP_001243794.1:n.-130-9732C>A
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