Canonical Allele Identifier: CA377098746

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571380T>C (hg19) ; chr10:g.67811622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811622T>C , CM000672.2:g.67811622T>C	GRCh38
NC_000010.10:g.69571380T>C , CM000672.1:g.69571380T>C	GRCh37
NC_000010.9:g.69241386T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.199A>G MANE Select	ENSP00000225171.2:p.Thr67Ala
ENST00000225171.6:c.199A>G	ENSP00000225171.2:p.Thr67Ala
ENST00000339758.7:c.199A>G	ENSP00000343575.6:p.Thr67Ala
ENST00000480180.1:c.*218A>G	ENSP00000474804.1:n.*218A>G
ENST00000480963.5:c.*119A>G	ENSP00000473979.1:n.*119A>G
ENST00000483798.6:c.289A>G	ENSP00000474215.1:p.Thr97Ala
NM_021800.2:c.199A>G	NP_068572.1:p.Thr67Ala
NM_201262.1:c.199A>G	NP_957714.1:p.Thr67Ala
XM_011539967.1:c.229A>G	XP_011538269.1:p.Thr77Ala
XM_017016431.1:c.-48A>G	XP_016871920.1:n.-48A>G
XM_017016432.2:c.-48A>G	XP_016871921.1:n.-48A>G
NM_021800.3:c.199A>G MANE Select	NP_068572.1:p.Thr67Ala
NM_201262.2:c.199A>G	NP_957714.1:p.Thr67Ala