Canonical Allele Identifier: CA1586100247
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947272G= , CM000667.2:g.138947272G= GRCh38
NC_000005.9:g.138282961G= , CM000667.1:g.138282961G= GRCh37
NC_000005.8:g.138310860G= NCBI36
NG_008112.1:g.256105C=
NG_008112.2:g.256105C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.1231C= MANE Select ENSP00000378294.2:p.Arg411=
ENST00000265195.9:c.1231C= ENSP00000265195.5:p.Arg411=
ENST00000394817.6:c.1231C= ENSP00000378294.2:p.Arg411=
ENST00000509534.5:c.1252C= ENSP00000426858.1:p.Arg418=
ENST00000515008.1:n.566C=
NM_001037633.1:c.1231C= NP_001032722.1:p.Arg411=
NM_022464.4:c.1231C= NP_071909.1:p.Arg411=
XM_011543570.1:c.1261C= XP_011541872.1:p.Arg421=
XM_011543570.2:c.1261C= XP_011541872.1:p.Arg421=
XM_024446164.1:c.1231C= XP_024301932.1:p.Arg411=
NM_022464.5:c.1231C= MANE Select NP_071909.1:p.Arg411=
NM_001037633.2:c.1231C= NP_001032722.1:p.Arg411=