Canonical Allele Identifier: CA370166170
Gene: DNAJB6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.157367439G>T , CM000669.2:g.157367439G>T GRCh38
NC_000007.13:g.157160133G>T , CM000669.1:g.157160133G>T GRCh37
NC_000007.12:g.156852894G>T NCBI36
NG_032573.1:g.35424G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262177.9:c.302G>T MANE Select ENSP00000262177.4:p.Arg101Met
ENST00000262177.8:c.302G>T ENSP00000262177.4:p.Arg101Met
ENST00000412557.5:c.302G>T ENSP00000403407.1:p.Arg101Met
ENST00000417758.5:c.302G>T ENSP00000400665.1:p.Arg101Met
ENST00000429029.6:c.302G>T ENSP00000397556.2:p.Arg101Met
ENST00000441291.5:c.302G>T ENSP00000415201.1:p.Arg101Met
ENST00000441561.5:c.302G>T ENSP00000410643.1:p.Arg101Met
ENST00000443280.5:c.302G>T ENSP00000396267.1:p.Arg101Met
ENST00000459889.5:c.302G>T ENSP00000488263.1:p.Arg101Met
ENST00000486083.6:n.469G>T
ENST00000488001.5:n.448G>T
ENST00000634080.1:c.302G>T ENSP00000488740.1:p.Arg101Met
NM_005494.2:c.302G>T NP_005485.1:p.Arg101Met
NM_058246.3:c.302G>T NP_490647.1:p.Arg101Met
XM_005249515.2:c.302G>T XP_005249572.1:p.Arg101Met
XM_005249516.2:c.302G>T XP_005249573.1:p.Arg101Met
XM_006715823.1:c.302G>T XP_006715886.1:p.Arg101Met
XM_011515704.1:c.302G>T XP_011514006.1:p.Arg101Met
NM_001363676.1:c.302G>T NP_001350605.1:p.Arg101Met
XM_005249515.3:c.302G>T XP_005249572.1:p.Arg101Met
XM_006715823.2:c.302G>T XP_006715886.1:p.Arg101Met
NM_058246.4:c.302G>T MANE Select NP_490647.1:p.Arg101Met
NM_005494.3:c.302G>T NP_005485.1:p.Arg101Met