Canonical Allele Identifier: CA377098575

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571305C>A (hg19) ; chr10:g.67811547C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811547C>A , CM000672.2:g.67811547C>A	GRCh38
NC_000010.10:g.69571305C>A , CM000672.1:g.69571305C>A	GRCh37
NC_000010.9:g.69241311C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.274G>T MANE Select	ENSP00000225171.2:p.Ala92Ser
ENST00000225171.6:c.274G>T	ENSP00000225171.2:p.Ala92Ser
ENST00000339758.7:c.274G>T	ENSP00000343575.6:p.Ala92Ser
ENST00000480180.1:c.*293G>T	ENSP00000474804.1:n.*293G>T
ENST00000480963.5:c.*194G>T	ENSP00000473979.1:n.*194G>T
ENST00000483798.6:c.364G>T	ENSP00000474215.1:p.Ala122Ser
NM_021800.2:c.274G>T	NP_068572.1:p.Ala92Ser
NM_201262.1:c.274G>T	NP_957714.1:p.Ala92Ser
XM_011539967.1:c.304G>T	XP_011538269.1:p.Ala102Ser
XM_017016431.1:c.28G>T	XP_016871920.1:p.Ala10Ser
XM_017016432.2:c.28G>T	XP_016871921.1:p.Ala10Ser
NM_021800.3:c.274G>T MANE Select	NP_068572.1:p.Ala92Ser
NM_201262.2:c.274G>T	NP_957714.1:p.Ala92Ser