Canonical Allele Identifier: CA377098514

Gene: DNAJC12

Linked Data

• gnomAD v4: 10-67811516-A-G
• MyVariant Identifiers: chr10:g.69571274A>G (hg19) ; chr10:g.67811516A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811516A>G , CM000672.2:g.67811516A>G	GRCh38
NC_000010.10:g.69571274A>G , CM000672.1:g.69571274A>G	GRCh37
NC_000010.9:g.69241280A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.297+8T>C MANE Select	ENSP00000225171.2:n.297+8T>C
ENST00000225171.6:c.297+8T>C	ENSP00000225171.2:n.297+8T>C
ENST00000339758.7:c.305T>C	ENSP00000343575.6:p.Phe102Ser
ENST00000480963.5:c.*217+8T>C	ENSP00000473979.1:n.*217+8T>C
ENST00000483798.6:c.387+8T>C	ENSP00000474215.1:n.387+8T>C
NM_021800.2:c.297+8T>C	NP_068572.1:n.297+8T>C
NM_201262.1:c.305T>C	NP_957714.1:p.Phe102Ser
XM_011539967.1:c.327+8T>C	XP_011538269.1:n.327+8T>C
XM_017016431.1:c.51+8T>C	XP_016871920.1:n.51+8T>C
XM_017016432.2:c.51+8T>C	XP_016871921.1:n.51+8T>C
NM_021800.3:c.297+8T>C MANE Select	NP_068572.1:n.297+8T>C
NM_201262.2:c.305T>C	NP_957714.1:p.Phe102Ser