Canonical Allele Identifier: CA469970059

Gene: DNAJC12

Linked Data

• dbSNP Id: rs1841859207
• MyVariant Identifiers: chr10:g.69571318G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811560G>A , CM000672.2:g.67811560G>A	GRCh38
NC_000010.10:g.69571318G>A , CM000672.1:g.69571318G>A	GRCh37
NC_000010.9:g.69241324G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.261C>T MANE Select	ENSP00000225171.2:p.Phe87=
ENST00000225171.6:c.261C>T	ENSP00000225171.2:p.Phe87=
ENST00000339758.7:c.261C>T	ENSP00000343575.6:p.Phe87=
ENST00000480180.1:c.*280C>T	ENSP00000474804.1:n.*280C>T
ENST00000480963.5:c.*181C>T	ENSP00000473979.1:n.*181C>T
ENST00000483798.6:c.351C>T	ENSP00000474215.1:p.Phe117=
NM_021800.2:c.261C>T	NP_068572.1:p.Phe87=
NM_201262.1:c.261C>T	NP_957714.1:p.Phe87=
XM_011539967.1:c.291C>T	XP_011538269.1:p.Phe97=
XM_017016431.1:c.15C>T	XP_016871920.1:p.Phe5=
XM_017016432.2:c.15C>T	XP_016871921.1:p.Phe5=
NM_021800.3:c.261C>T MANE Select	NP_068572.1:p.Phe87=
NM_201262.2:c.261C>T	NP_957714.1:p.Phe87=