Canonical Allele Identifier: CA469970045

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571288C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811530C>G , CM000672.2:g.67811530C>G	GRCh38
NC_000010.10:g.69571288C>G , CM000672.1:g.69571288C>G	GRCh37
NC_000010.9:g.69241294C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.291G>C MANE Select	ENSP00000225171.2:p.Val97=
ENST00000225171.6:c.291G>C	ENSP00000225171.2:p.Val97=
ENST00000339758.7:c.291G>C	ENSP00000343575.6:p.Val97=
ENST00000480180.1:c.*310G>C	ENSP00000474804.1:n.*310G>C
ENST00000480963.5:c.*211G>C	ENSP00000473979.1:n.*211G>C
ENST00000483798.6:c.381G>C	ENSP00000474215.1:p.Val127=
NM_021800.2:c.291G>C	NP_068572.1:p.Val97=
NM_201262.1:c.291G>C	NP_957714.1:p.Val97=
XM_011539967.1:c.321G>C	XP_011538269.1:p.Val107=
XM_017016431.1:c.45G>C	XP_016871920.1:p.Val15=
XM_017016432.2:c.45G>C	XP_016871921.1:p.Val15=
NM_021800.3:c.291G>C MANE Select	NP_068572.1:p.Val97=
NM_201262.2:c.291G>C	NP_957714.1:p.Val97=