Canonical Allele Identifier: CA6552225
Gene: DNAJC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49349383G>C , CM000674.2:g.49349383G>C GRCh38
NC_000012.11:g.49743166G>C , CM000674.1:g.49743166G>C GRCh37
NC_000012.10:g.48029433G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001304944.2:c.511G>C MANE Select NP_001291873.1:p.Ala171Pro
ENST00000549441.7:c.511G>C MANE Select ENSP00000446830.1:p.Ala171Pro
NM_001304944.1:c.511G>C NP_001291873.1:p.Ala171Pro
NM_024902.3:c.511G>C NP_079178.2:p.Ala171Pro
NM_024902.4:c.511G>C NP_079178.2:p.Ala171Pro
ENST00000395069.3:c.511G>C ENSP00000378508.2:p.Ala171Pro
ENST00000549441.6:c.511G>C ENSP00000446830.1:p.Ala171Pro
ENST00000647553.1:c.511G>C ENSP00000498036.1:p.Ala171Pro
XM_005269155.2:c.511G>C XP_005269212.1:p.Ala171Pro
XM_005269156.2:c.511G>C XP_005269213.1:p.Ala171Pro
XM_005269157.2:c.511G>C XP_005269214.1:p.Ala171Pro