Canonical Allele Identifier: CA10649487
Gene: SCO1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10680799T= , CM000679.2:g.10680799T= GRCh38
NG_008228.2:g.21770A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255390.10:c.*320A= MANE Select ENSP00000255390.5:n.*320A=
ENST00000577335.2:c.*1048A= ENSP00000464032.1:n.*1048A=
ENST00000255390.9:c.*320A= ENSP00000255390.5:n.*320A=
ENST00000577427.1:c.*320A= ENSP00000463387.1:n.*320A=
NM_004589.3:c.*320A= NP_004580.1:n.*320A=
XM_005256751.2:c.*320A= XP_005256808.1:n.*320A=
XM_005256751.4:c.*320A= XP_005256808.1:n.*320A=
NM_004589.4:c.*320A= MANE Select NP_004580.1:n.*320A=
Search 100 bp 5'
Search 100 bp 3'