Canonical Allele Identifier: CA667760157

Gene: DNAJC12

Linked Data

• dbSNP Id: rs746006867
• gnomAD v3: 10-67811512-C-A
• gnomAD v4: 10-67811512-C-A
• MyVariant Identifiers: chr10:g.69571270C>A (hg19) ; chr10:g.67811512C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811512C>A , CM000672.2:g.67811512C>A	GRCh38
NC_000010.10:g.69571270C>A , CM000672.1:g.69571270C>A	GRCh37
NC_000010.9:g.69241276C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.297+12G>T MANE Select	ENSP00000225171.2:n.297+12G>T
ENST00000225171.6:c.297+12G>T	ENSP00000225171.2:n.297+12G>T
ENST00000339758.7:c.309G>T	ENSP00000343575.6:p.Ser103=
ENST00000480963.5:c.*217+12G>T	ENSP00000473979.1:n.*217+12G>T
ENST00000483798.6:c.387+12G>T	ENSP00000474215.1:n.387+12G>T
NM_021800.2:c.297+12G>T	NP_068572.1:n.297+12G>T
NM_201262.1:c.309G>T	NP_957714.1:p.Ser103=
XM_011539967.1:c.327+12G>T	XP_011538269.1:n.327+12G>T
XM_017016431.1:c.51+12G>T	XP_016871920.1:n.51+12G>T
XM_017016432.2:c.51+12G>T	XP_016871921.1:n.51+12G>T
NM_021800.3:c.297+12G>T MANE Select	NP_068572.1:n.297+12G>T
NM_201262.2:c.309G>T	NP_957714.1:p.Ser103=