Canonical Allele Identifier: CA2326567901

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18869412C= , CM000681.2:g.18869412C= GRCh38
NC_000019.9:g.18980221C= , CM000681.1:g.18980221C= GRCh37
NC_000019.8:g.18841221C= NCBI36
NG_012070.1:g.31733G=
NG_033056.1:g.31733G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623882.4:c.*595-22G= (CERS1) MANE Select ENSP00000485308.1:n.*595-22G=
ENST00000247005.8:c.326-22G= (GDF1) MANE Select ENSP00000247005.5:n.326-22G=
ENST00000247005.7:c.326-22G= (GDF1) ENSP00000247005.5:n.326-22G=
ENST00000623882.3:c.*595-22G= (CERS1) ENSP00000485308.1:n.*595-22G=
ENST00000623927.1:c.326-22G= (CERS1) ENSP00000485582.1:n.326-22G=
NM_001492.5:c.326-22G= (GDF1) NP_001483.3:n.326-22G=
NM_021267.4:c.*595-22G= (CERS1) NP_067090.1:n.*595-22G=
NM_001492.6:c.326-22G= (GDF1) MANE Select NP_001483.3:n.326-22G=
NM_021267.5:c.*595-22G= (CERS1) MANE Select NP_067090.1:n.*595-22G=
NM_001387438.1:c.326-22G= (GDF1) NP_001374367.1:n.326-22G=
NM_001387440.1:c.*1165G= (CERS1) NP_001374369.1:n.*1165G=