Canonical Allele Identifier: CA1172265572
Gene: DNAJC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65349976C>G , CM000663.2:g.65349976C>G GRCh38
NC_000001.10:g.65815659C>G , CM000663.1:g.65815659C>G GRCh37
NC_000001.9:g.65588247C>G NCBI36
NG_033843.1:g.90283C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371069.5:c.194-14659C>G MANE Select ENSP00000360108.4:n.194-14659C>G
ENST00000263441.11:c.-18+4253C>G ENSP00000263441.7:n.-18+4253C>G
ENST00000371069.4:c.194-14659C>G ENSP00000360108.4:n.194-14659C>G
ENST00000395325.7:c.23-14659C>G ENSP00000378735.3:n.23-14659C>G
ENST00000463018.5:n.198+4253C>G
ENST00000483402.1:n.282+4253C>G
ENST00000494710.6:c.116-14659C>G ENSP00000473821.1:n.116-14659C>G
NM_001256864.1:c.194-14659C>G NP_001243793.1:n.194-14659C>G
NM_001256865.1:c.-18+4253C>G NP_001243794.1:n.-18+4253C>G
NM_014787.3:c.23-14659C>G NP_055602.1:n.23-14659C>G
XM_011542483.1:c.143-14659C>G XP_011540785.1:n.143-14659C>G
XM_011542484.1:c.116-14659C>G XP_011540786.1:n.116-14659C>G
XM_011542485.1:c.29-14659C>G XP_011540787.1:n.29-14659C>G
XM_011542486.1:c.-18+4253C>G XP_011540788.1:n.-18+4253C>G
XM_011542487.1:c.-18+4253C>G XP_011540789.1:n.-18+4253C>G
XM_011542488.1:c.-18+4253C>G XP_011540790.1:n.-18+4253C>G
NM_001256864.2:c.194-14659C>G MANE Select NP_001243793.1:n.194-14659C>G
NM_014787.4:c.23-14659C>G NP_055602.1:n.23-14659C>G
NM_001256865.2:c.-18+4253C>G NP_001243794.1:n.-18+4253C>G