Canonical Allele Identifier: CA377098761

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571388T>A (hg19) ; chr10:g.67811630T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811630T>A , CM000672.2:g.67811630T>A	GRCh38
NC_000010.10:g.69571388T>A , CM000672.1:g.69571388T>A	GRCh37
NC_000010.9:g.69241394T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.191A>T MANE Select	ENSP00000225171.2:p.Glu64Val
ENST00000225171.6:c.191A>T	ENSP00000225171.2:p.Glu64Val
ENST00000339758.7:c.191A>T	ENSP00000343575.6:p.Glu64Val
ENST00000480180.1:c.*210A>T	ENSP00000474804.1:n.*210A>T
ENST00000480963.5:c.*111A>T	ENSP00000473979.1:n.*111A>T
ENST00000483798.6:c.281A>T	ENSP00000474215.1:p.Glu94Val
NM_021800.2:c.191A>T	NP_068572.1:p.Glu64Val
NM_201262.1:c.191A>T	NP_957714.1:p.Glu64Val
XM_011539967.1:c.221A>T	XP_011538269.1:p.Glu74Val
XM_017016431.1:c.-56A>T	XP_016871920.1:n.-56A>T
XM_017016432.2:c.-56A>T	XP_016871921.1:n.-56A>T
NM_021800.3:c.191A>T MANE Select	NP_068572.1:p.Glu64Val
NM_201262.2:c.191A>T	NP_957714.1:p.Glu64Val