Canonical Allele Identifier: CA377098663

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571340C>A (hg19) ; chr10:g.67811582C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811582C>A , CM000672.2:g.67811582C>A	GRCh38
NC_000010.10:g.69571340C>A , CM000672.1:g.69571340C>A	GRCh37
NC_000010.9:g.69241346C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.239G>T MANE Select	ENSP00000225171.2:p.Arg80Met
ENST00000225171.6:c.239G>T	ENSP00000225171.2:p.Arg80Met
ENST00000339758.7:c.239G>T	ENSP00000343575.6:p.Arg80Met
ENST00000480180.1:c.*258G>T	ENSP00000474804.1:n.*258G>T
ENST00000480963.5:c.*159G>T	ENSP00000473979.1:n.*159G>T
ENST00000483798.6:c.329G>T	ENSP00000474215.1:p.Arg110Met
NM_021800.2:c.239G>T	NP_068572.1:p.Arg80Met
NM_201262.1:c.239G>T	NP_957714.1:p.Arg80Met
XM_011539967.1:c.269G>T	XP_011538269.1:p.Arg90Met
XM_017016431.1:c.-8G>T	XP_016871920.1:n.-8G>T
XM_017016432.2:c.-8G>T	XP_016871921.1:n.-8G>T
NM_021800.3:c.239G>T MANE Select	NP_068572.1:p.Arg80Met
NM_201262.2:c.239G>T	NP_957714.1:p.Arg80Met