Canonical Allele Identifier: CA1586100076
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946900C= , CM000667.2:g.138946900C= GRCh38
NC_000005.9:g.138282589C= , CM000667.1:g.138282589C= GRCh37
NC_000005.8:g.138310488C= NCBI36
NG_008112.1:g.256477G=
NG_008112.2:g.256477G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*217G= MANE Select ENSP00000378294.2:n.*217G=
ENST00000265195.9:c.*217G= ENSP00000265195.5:n.*217G=
ENST00000394817.6:c.*217G= ENSP00000378294.2:n.*217G=
NM_001037633.1:c.*217G= NP_001032722.1:n.*217G=
NM_022464.4:c.*217G= NP_071909.1:n.*217G=
XM_011543570.2:c.*217G= XP_011541872.1:n.*217G=
XM_024446164.1:c.*217G= XP_024301932.1:n.*217G=
NM_022464.5:c.*217G= MANE Select NP_071909.1:n.*217G=
NM_001037633.2:c.*217G= NP_001032722.1:n.*217G=