Canonical Allele Identifier: CA1917049464

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811558_67811559delinsTG , CM000672.2:g.67811558_67811559delinsTG	GRCh38
NC_000010.10:g.69571316_69571317delinsTG , CM000672.1:g.69571316_69571317delinsTG	GRCh37
NC_000010.9:g.69241322_69241323delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.262_263delinsCA MANE Select	ENSP00000225171.2:p.Gln88=
ENST00000225171.6:c.262_263delinsCA	ENSP00000225171.2:p.Gln88=
ENST00000339758.7:c.262_263delinsCA	ENSP00000343575.6:p.Gln88=
ENST00000480180.1:c.*281_*282delinsCA	ENSP00000474804.1:n.*281_*282delinsCA
ENST00000480963.5:c.*182_*183delinsCA	ENSP00000473979.1:n.*182_*183delinsCA
ENST00000483798.6:c.352_353delinsCA	ENSP00000474215.1:p.Gln118=
NM_021800.2:c.262_263delinsCA	NP_068572.1:p.Gln88=
NM_201262.1:c.262_263delinsCA	NP_957714.1:p.Gln88=
XM_011539967.1:c.292_293delinsCA	XP_011538269.1:p.Gln98=
XM_017016431.1:c.16_17delinsCA	XP_016871920.1:p.Gln6=
XM_017016432.2:c.16_17delinsCA	XP_016871921.1:p.Gln6=
NM_021800.3:c.262_263delinsCA MANE Select	NP_068572.1:p.Gln88=
NM_201262.2:c.262_263delinsCA	NP_957714.1:p.Gln88=