Canonical Allele Identifier: CA816234359
Gene: SIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.100388364del , CM000668.2:g.100388364del GRCh38
NC_000006.11:g.100836240del , CM000668.1:g.100836240del GRCh37
NC_000006.10:g.100942961del NCBI36
NG_008230.1:g.80319del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369208.8:c.*2004del MANE Select ENSP00000358210.4:n.*2004del
ENST00000369208.7:c.*2004del ENSP00000358210.3:n.*2004del
XM_005267100.2:c.*2004del XP_005267157.1:n.*2004del
XM_017011197.1:c.*2004del XP_016866686.1:n.*2004del
NM_001374769.1:c.*2004del NP_001361698.1:n.*2004del
NM_005068.3:c.*2004del MANE Select NP_005059.2:n.*2004del