Canonical Allele Identifier: CA5520892

Gene: DNAJC12

Linked Data

• dbSNP Id: rs747131362
• ExAC: 10:69571449 T / C
• gnomAD v2: 10-69571449-T-C
• gnomAD v3: 10-67811691-T-C
• gnomAD v4: 10-67811691-T-C
• MyVariant Identifiers: chr10:g.69571449T>C (hg19) ; chr10:g.67811691T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811691T>C , CM000672.2:g.67811691T>C	GRCh38
NC_000010.10:g.69571449T>C , CM000672.1:g.69571449T>C	GRCh37
NC_000010.9:g.69241455T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.158-28A>G MANE Select	ENSP00000225171.2:n.158-28A>G
ENST00000225171.6:c.158-28A>G	ENSP00000225171.2:n.158-28A>G
ENST00000339758.7:c.158-28A>G	ENSP00000343575.6:n.158-28A>G
ENST00000480180.1:c.*177-28A>G	ENSP00000474804.1:n.*177-28A>G
ENST00000480963.5:c.*78-28A>G	ENSP00000473979.1:n.*78-28A>G
ENST00000483798.6:c.248-28A>G	ENSP00000474215.1:n.248-28A>G
NM_021800.2:c.158-28A>G	NP_068572.1:n.158-28A>G
NM_201262.1:c.158-28A>G	NP_957714.1:n.158-28A>G
XM_011539967.1:c.188-28A>G	XP_011538269.1:n.188-28A>G
XM_017016431.1:c.-89-28A>G	XP_016871920.1:n.-89-28A>G
XM_017016432.2:c.-89-28A>G	XP_016871921.1:n.-89-28A>G
NM_021800.3:c.158-28A>G MANE Select	NP_068572.1:n.158-28A>G
NM_201262.2:c.158-28A>G	NP_957714.1:n.158-28A>G