Canonical Allele Identifier: CA377098502

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571268A>T (hg19) ; chr10:g.67811510A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811510A>T , CM000672.2:g.67811510A>T	GRCh38
NC_000010.10:g.69571268A>T , CM000672.1:g.69571268A>T	GRCh37
NC_000010.9:g.69241274A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.297+14T>A MANE Select	ENSP00000225171.2:n.297+14T>A
ENST00000225171.6:c.297+14T>A	ENSP00000225171.2:n.297+14T>A
ENST00000339758.7:c.311T>A	ENSP00000343575.6:p.Leu104Gln
ENST00000480963.5:c.*217+14T>A	ENSP00000473979.1:n.*217+14T>A
ENST00000483798.6:c.387+14T>A	ENSP00000474215.1:n.387+14T>A
NM_021800.2:c.297+14T>A	NP_068572.1:n.297+14T>A
NM_201262.1:c.311T>A	NP_957714.1:p.Leu104Gln
XM_011539967.1:c.327+14T>A	XP_011538269.1:n.327+14T>A
XM_017016431.1:c.51+14T>A	XP_016871920.1:n.51+14T>A
XM_017016432.2:c.51+14T>A	XP_016871921.1:n.51+14T>A
NM_021800.3:c.297+14T>A MANE Select	NP_068572.1:n.297+14T>A
NM_201262.2:c.311T>A	NP_957714.1:p.Leu104Gln