Canonical Allele Identifier: CA377098553

Gene: DNAJC12

Linked Data

• gnomAD v4: 10-67811536-G-C
• MyVariant Identifiers: chr10:g.69571294G>C (hg19) ; chr10:g.67811536G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811536G>C , CM000672.2:g.67811536G>C	GRCh38
NC_000010.10:g.69571294G>C , CM000672.1:g.69571294G>C	GRCh37
NC_000010.9:g.69241300G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.285C>G MANE Select	ENSP00000225171.2:p.Asp95Glu
ENST00000225171.6:c.285C>G	ENSP00000225171.2:p.Asp95Glu
ENST00000339758.7:c.285C>G	ENSP00000343575.6:p.Asp95Glu
ENST00000480180.1:c.*304C>G	ENSP00000474804.1:n.*304C>G
ENST00000480963.5:c.*205C>G	ENSP00000473979.1:n.*205C>G
ENST00000483798.6:c.375C>G	ENSP00000474215.1:p.Asp125Glu
NM_021800.2:c.285C>G	NP_068572.1:p.Asp95Glu
NM_201262.1:c.285C>G	NP_957714.1:p.Asp95Glu
XM_011539967.1:c.315C>G	XP_011538269.1:p.Asp105Glu
XM_017016431.1:c.39C>G	XP_016871920.1:p.Asp13Glu
XM_017016432.2:c.39C>G	XP_016871921.1:p.Asp13Glu
NM_021800.3:c.285C>G MANE Select	NP_068572.1:p.Asp95Glu
NM_201262.2:c.285C>G	NP_957714.1:p.Asp95Glu