Canonical Allele Identifier: CA1574830

Gene: DNAJC5G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27277876A>G , CM000664.2:g.27277876A>G	GRCh38
NC_000002.11:g.27500744A>G , CM000664.1:g.27500744A>G	GRCh37
NC_000002.10:g.27354248A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173650.3:c.236A>G MANE Select	NP_775921.1:p.Asn79Ser
ENST00000296097.8:c.236A>G MANE Select	ENSP00000296097.3:p.Asn79Ser
NM_001303127.1:c.236A>G	NP_001290056.1:p.Asn79Ser
NM_001303127.2:c.236A>G	NP_001290056.1:p.Asn79Ser
NM_001303128.1:c.114-312A>G	NP_001290057.1:n.114-312A>G
NM_001303128.2:c.114-312A>G	NP_001290057.1:n.114-312A>G
NM_173650.2:c.236A>G	NP_775921.1:p.Asn79Ser
NR_130126.1:n.152-312A>G
NR_130126.2:n.140-312A>G
ENST00000296097.7:c.236A>G	ENSP00000296097.3:p.Asn79Ser
ENST00000402462.5:c.236A>G	ENSP00000384305.1:p.Asn79Ser
ENST00000404433.5:c.188A>G	ENSP00000385829.1:p.Asn63Ser
ENST00000406962.1:c.114-312A>G	ENSP00000385533.1:n.114-312A>G
ENST00000420191.5:c.114-312A>G	ENSP00000400382.1:n.114-312A>G
XM_006711995.2:c.236A>G	XP_006712058.1:p.Asn79Ser
XM_006711995.3:c.236A>G	XP_006712058.1:p.Asn79Ser
XM_017003872.2:c.236A>G	XP_016859361.1:p.Asn79Ser
XM_017003873.2:c.236A>G	XP_016859362.1:p.Asn79Ser
XM_017003874.2:c.236A>G	XP_016859363.1:p.Asn79Ser