Canonical Allele Identifier: CA10575852
Community Standard Title: NM_001012339.3(DNAJC21):c.94C>G (p.Pro32Ala)
Gene: DNAJC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34929913C>G , CM000667.2:g.34929913C>G GRCh38
NC_000005.9:g.34930018C>G , CM000667.1:g.34930018C>G GRCh37
NC_000005.8:g.34965775C>G NCBI36
NG_052822.1:g.5374C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001012339.3:c.94C>G MANE Select NP_001012339.2:p.Pro32Ala
ENST00000648817.1:c.94C>G MANE Select ENSP00000497410.1:p.Pro32Ala
NM_001012339.2:c.94C>G NP_001012339.2:p.Pro32Ala
NM_001348420.1:c.94C>G NP_001335349.1:p.Pro32Ala
NM_001348420.2:c.94C>G NP_001335349.1:p.Pro32Ala
NM_194283.3:c.94C>G NP_919259.3:p.Pro32Ala
NM_194283.4:c.94C>G NP_919259.3:p.Pro32Ala
ENST00000342382.8:c.94C>G ENSP00000343728.4:p.Pro32Ala
ENST00000382021.2:c.94C>G ENSP00000371451.2:p.Pro32Ala
ENST00000506762.2:c.-255C>G ENSP00000513864.1:n.-255C>G
ENST00000512136.2:n.321C>G
ENST00000642851.1:c.94C>G ENSP00000496545.1:p.Pro32Ala
XM_005248249.3:c.94C>G XP_005248306.1:p.Pro32Ala
XM_005248250.2:c.94C>G XP_005248307.1:p.Pro32Ala
XM_005248250.3:c.355C>G XP_005248307.2:p.Pro119Ala
XM_011513965.1:c.94C>G XP_011512267.1:p.Pro32Ala
XM_011513965.2:c.355C>G XP_011512267.2:p.Pro119Ala
XM_011513966.1:c.94C>G XP_011512268.1:p.Pro32Ala
XM_011513966.2:c.355C>G XP_011512268.2:p.Pro119Ala