Canonical Allele Identifier: CA2788369898
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811414C>A , CM000672.2:g.67811414C>A GRCh38
NC_000010.10:g.69571172C>A , CM000672.1:g.69571172C>A GRCh37
NC_000010.9:g.69241178C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.297+110G>T MANE Select ENSP00000225171.2:n.297+110G>T
ENST00000225171.6:c.297+110G>T ENSP00000225171.2:n.297+110G>T
ENST00000339758.7:c.*83G>T ENSP00000343575.6:n.*83G>T
ENST00000480963.5:c.*217+110G>T ENSP00000473979.1:n.*217+110G>T
ENST00000483798.6:c.387+110G>T ENSP00000474215.1:n.387+110G>T
NM_021800.2:c.297+110G>T NP_068572.1:n.297+110G>T
NM_201262.1:c.*83G>T NP_957714.1:n.*83G>T
XM_011539967.1:c.327+110G>T XP_011538269.1:n.327+110G>T
XM_017016431.1:c.51+110G>T XP_016871920.1:n.51+110G>T
XM_017016432.2:c.51+110G>T XP_016871921.1:n.51+110G>T
NM_021800.3:c.297+110G>T MANE Select NP_068572.1:n.297+110G>T
NM_201262.2:c.*83G>T NP_957714.1:n.*83G>T