Canonical Allele Identifier: CA1586100111
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946971C= , CM000667.2:g.138946971C= GRCh38
NC_000005.9:g.138282660C= , CM000667.1:g.138282660C= GRCh37
NC_000005.8:g.138310559C= NCBI36
NG_008112.1:g.256406G=
NG_008112.2:g.256406G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*146G= MANE Select ENSP00000378294.2:n.*146G=
ENST00000265195.9:c.*146G= ENSP00000265195.5:n.*146G=
ENST00000394817.6:c.*146G= ENSP00000378294.2:n.*146G=
NM_001037633.1:c.*146G= NP_001032722.1:n.*146G=
NM_022464.4:c.*146G= NP_071909.1:n.*146G=
XM_011543570.2:c.*146G= XP_011541872.1:n.*146G=
XM_024446164.1:c.*146G= XP_024301932.1:n.*146G=
NM_022464.5:c.*146G= MANE Select NP_071909.1:n.*146G=
NM_001037633.2:c.*146G= NP_001032722.1:n.*146G=