Canonical Allele Identifier: CA377098622

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571323G>C (hg19) ; chr10:g.67811565G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811565G>C , CM000672.2:g.67811565G>C	GRCh38
NC_000010.10:g.69571323G>C , CM000672.1:g.69571323G>C	GRCh37
NC_000010.9:g.69241329G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.256C>G MANE Select	ENSP00000225171.2:p.Pro86Ala
ENST00000225171.6:c.256C>G	ENSP00000225171.2:p.Pro86Ala
ENST00000339758.7:c.256C>G	ENSP00000343575.6:p.Pro86Ala
ENST00000480180.1:c.*275C>G	ENSP00000474804.1:n.*275C>G
ENST00000480963.5:c.*176C>G	ENSP00000473979.1:n.*176C>G
ENST00000483798.6:c.346C>G	ENSP00000474215.1:p.Pro116Ala
NM_021800.2:c.256C>G	NP_068572.1:p.Pro86Ala
NM_201262.1:c.256C>G	NP_957714.1:p.Pro86Ala
XM_011539967.1:c.286C>G	XP_011538269.1:p.Pro96Ala
XM_017016431.1:c.10C>G	XP_016871920.1:p.Pro4Ala
XM_017016432.2:c.10C>G	XP_016871921.1:p.Pro4Ala
NM_021800.3:c.256C>G MANE Select	NP_068572.1:p.Pro86Ala
NM_201262.2:c.256C>G	NP_957714.1:p.Pro86Ala