Canonical Allele Identifier: CA4590583
Gene: DNAJB6 HGNC NCBI
gnomAD v4:
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.157385523T>A , CM000669.2:g.157385523T>A GRCh38
NC_000007.13:g.157178217T>A , CM000669.1:g.157178217T>A GRCh37
NC_000007.12:g.156870978T>A NCBI36
NG_032573.1:g.53508T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262177.9:c.621-18T>A MANE Select ENSP00000262177.4:n.621-18T>A
ENST00000262177.8:c.621-18T>A ENSP00000262177.4:n.621-18T>A
ENST00000417758.5:c.621-18T>A ENSP00000400665.1:n.621-18T>A
ENST00000429029.6:c.621-18T>A ENSP00000397556.2:n.621-18T>A
ENST00000443280.5:c.346+18040T>A ENSP00000396267.1:n.346+18040T>A
ENST00000459889.5:c.621-18T>A ENSP00000488263.1:n.621-18T>A
ENST00000465908.5:n.417-18T>A
ENST00000487480.1:n.4396-18T>A
ENST00000634080.1:c.621-18T>A ENSP00000488740.1:n.621-18T>A
NM_005494.2:c.621-18T>A NP_005485.1:n.621-18T>A
NM_058246.3:c.621-18T>A NP_490647.1:n.621-18T>A
XM_005249515.2:c.621-18T>A XP_005249572.1:n.621-18T>A
XM_005249516.2:c.621-18T>A XP_005249573.1:n.621-18T>A
XM_006715823.1:c.621-18T>A XP_006715886.1:n.621-18T>A
XM_011515704.1:c.621-18T>A XP_011514006.1:n.621-18T>A
NM_001363676.1:c.346+18040T>A NP_001350605.1:n.346+18040T>A
XM_005249515.3:c.621-18T>A XP_005249572.1:n.621-18T>A
XM_006715823.2:c.621-18T>A XP_006715886.1:n.621-18T>A
NM_058246.4:c.621-18T>A MANE Select NP_490647.1:n.621-18T>A
NM_005494.3:c.621-18T>A NP_005485.1:n.621-18T>A