Canonical Allele Identifier: CA1586100176
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947103C= , CM000667.2:g.138947103C= GRCh38
NC_000005.9:g.138282792C= , CM000667.1:g.138282792C= GRCh37
NC_000005.8:g.138310691C= NCBI36
NG_008112.1:g.256274G=
NG_008112.2:g.256274G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*14G= MANE Select ENSP00000378294.2:n.*14G=
ENST00000265195.9:c.*14G= ENSP00000265195.5:n.*14G=
ENST00000394817.6:c.*14G= ENSP00000378294.2:n.*14G=
ENST00000509534.5:c.*14G= ENSP00000426858.1:n.*14G=
ENST00000515008.1:n.735G=
NM_001037633.1:c.*14G= NP_001032722.1:n.*14G=
NM_022464.4:c.*14G= NP_071909.1:n.*14G=
XM_011543570.1:c.*14G= XP_011541872.1:n.*14G=
XM_011543570.2:c.*14G= XP_011541872.1:n.*14G=
XM_024446164.1:c.*14G= XP_024301932.1:n.*14G=
NM_022464.5:c.*14G= MANE Select NP_071909.1:n.*14G=
NM_001037633.2:c.*14G= NP_001032722.1:n.*14G=