Canonical Allele Identifier: CA2326567766

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18869209T= , CM000681.2:g.18869209T= GRCh38
NC_000019.9:g.18980018T= , CM000681.1:g.18980018T= GRCh37
NC_000019.8:g.18841018T= NCBI36
NG_012070.1:g.31936A=
NG_033056.1:g.31936A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623882.4:c.*776A= (CERS1) MANE Select ENSP00000485308.1:n.*776A=
ENST00000247005.8:c.507A= (GDF1) MANE Select ENSP00000247005.5:p.Gln169=
ENST00000247005.7:c.507A= (GDF1) ENSP00000247005.5:p.Gln169=
ENST00000623882.3:c.*776A= (CERS1) ENSP00000485308.1:n.*776A=
ENST00000623927.1:c.507A= (CERS1) ENSP00000485582.1:p.Gln169=
NM_001492.5:c.507A= (GDF1) NP_001483.3:p.Gln169=
NM_021267.4:c.*776A= (CERS1) NP_067090.1:n.*776A=
NM_001492.6:c.507A= (GDF1) MANE Select NP_001483.3:p.Gln169=
NM_021267.5:c.*776A= (CERS1) MANE Select NP_067090.1:n.*776A=
NM_001387438.1:c.507A= (GDF1) NP_001374367.1:p.Gln169=
NM_001387440.1:c.*1368A= (CERS1) NP_001374369.1:n.*1368A=