Canonical Allele Identifier: CA2675501620
Gene: SIL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947031dup , CM000667.2:g.138947031dup GRCh38
NC_000005.9:g.138282720dup , CM000667.1:g.138282720dup GRCh37
NC_000005.8:g.138310619dup NCBI36
NG_008112.1:g.256347dup
NG_008112.2:g.256347dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*87dup MANE Select ENSP00000378294.2:n.*87dup
ENST00000265195.9:c.*87dup ENSP00000265195.5:n.*87dup
ENST00000394817.6:c.*87dup ENSP00000378294.2:n.*87dup
ENST00000509534.5:c.*87dup ENSP00000426858.1:n.*87dup
ENST00000515008.1:n.808dup
NM_001037633.1:c.*87dup NP_001032722.1:n.*87dup
NM_022464.4:c.*87dup NP_071909.1:n.*87dup
XM_011543570.1:c.*87dup XP_011541872.1:n.*87dup
XM_011543570.2:c.*87dup XP_011541872.1:n.*87dup
XM_024446164.1:c.*87dup XP_024301932.1:n.*87dup
NM_022464.5:c.*87dup MANE Select NP_071909.1:n.*87dup
NM_001037633.2:c.*87dup NP_001032722.1:n.*87dup