Canonical Allele Identifier: CA469970075
Gene: DNAJC12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69571360G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811602G>C , CM000672.2:g.67811602G>C GRCh38
NC_000010.10:g.69571360G>C , CM000672.1:g.69571360G>C GRCh37
NC_000010.9:g.69241366G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.219C>G MANE Select ENSP00000225171.2:p.Ala73=
ENST00000225171.6:c.219C>G ENSP00000225171.2:p.Ala73=
ENST00000339758.7:c.219C>G ENSP00000343575.6:p.Ala73=
ENST00000480180.1:c.*238C>G ENSP00000474804.1:n.*238C>G
ENST00000480963.5:c.*139C>G ENSP00000473979.1:n.*139C>G
ENST00000483798.6:c.309C>G ENSP00000474215.1:p.Ala103=
NM_021800.2:c.219C>G NP_068572.1:p.Ala73=
NM_201262.1:c.219C>G NP_957714.1:p.Ala73=
XM_011539967.1:c.249C>G XP_011538269.1:p.Ala83=
XM_017016431.1:c.-28C>G XP_016871920.1:n.-28C>G
XM_017016432.2:c.-28C>G XP_016871921.1:n.-28C>G
NM_021800.3:c.219C>G MANE Select NP_068572.1:p.Ala73=
NM_201262.2:c.219C>G NP_957714.1:p.Ala73=