Canonical Allele Identifier: CA469970058

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571315C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811557C>T , CM000672.2:g.67811557C>T	GRCh38
NC_000010.10:g.69571315C>T , CM000672.1:g.69571315C>T	GRCh37
NC_000010.9:g.69241321C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.264G>A MANE Select	ENSP00000225171.2:p.Gln88=
ENST00000225171.6:c.264G>A	ENSP00000225171.2:p.Gln88=
ENST00000339758.7:c.264G>A	ENSP00000343575.6:p.Gln88=
ENST00000480180.1:c.*283G>A	ENSP00000474804.1:n.*283G>A
ENST00000480963.5:c.*184G>A	ENSP00000473979.1:n.*184G>A
ENST00000483798.6:c.354G>A	ENSP00000474215.1:p.Gln118=
NM_021800.2:c.264G>A	NP_068572.1:p.Gln88=
NM_201262.1:c.264G>A	NP_957714.1:p.Gln88=
XM_011539967.1:c.294G>A	XP_011538269.1:p.Gln98=
XM_017016431.1:c.18G>A	XP_016871920.1:p.Gln6=
XM_017016432.2:c.18G>A	XP_016871921.1:p.Gln6=
NM_021800.3:c.264G>A MANE Select	NP_068572.1:p.Gln88=
NM_201262.2:c.264G>A	NP_957714.1:p.Gln88=