Canonical Allele Identifier: CA2326567785

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18869245T= , CM000681.2:g.18869245T= GRCh38
NC_000019.9:g.18980054T= , CM000681.1:g.18980054T= GRCh37
NC_000019.8:g.18841054T= NCBI36
NG_012070.1:g.31900A=
NG_033056.1:g.31900A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623882.4:c.*740A= (CERS1) MANE Select ENSP00000485308.1:n.*740A=
ENST00000247005.8:c.471A= (GDF1) MANE Select ENSP00000247005.5:p.Ala157=
ENST00000247005.7:c.471A= (GDF1) ENSP00000247005.5:p.Ala157=
ENST00000623882.3:c.*740A= (CERS1) ENSP00000485308.1:n.*740A=
ENST00000623927.1:c.471A= (CERS1) ENSP00000485582.1:p.Ala157=
NM_001492.5:c.471A= (GDF1) NP_001483.3:p.Ala157=
NM_021267.4:c.*740A= (CERS1) NP_067090.1:n.*740A=
NM_001492.6:c.471A= (GDF1) MANE Select NP_001483.3:p.Ala157=
NM_021267.5:c.*740A= (CERS1) MANE Select NP_067090.1:n.*740A=
NM_001387438.1:c.471A= (GDF1) NP_001374367.1:p.Ala157=
NM_001387440.1:c.*1332A= (CERS1) NP_001374369.1:n.*1332A=