Canonical Allele Identifier: CA1586100085
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946922A= , CM000667.2:g.138946922A= GRCh38
NC_000005.9:g.138282611A= , CM000667.1:g.138282611A= GRCh37
NC_000005.8:g.138310510A= NCBI36
NG_008112.1:g.256455T=
NG_008112.2:g.256455T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*195T= MANE Select ENSP00000378294.2:n.*195T=
ENST00000265195.9:c.*195T= ENSP00000265195.5:n.*195T=
ENST00000394817.6:c.*195T= ENSP00000378294.2:n.*195T=
NM_001037633.1:c.*195T= NP_001032722.1:n.*195T=
NM_022464.4:c.*195T= NP_071909.1:n.*195T=
XM_011543570.2:c.*195T= XP_011541872.1:n.*195T=
XM_024446164.1:c.*195T= XP_024301932.1:n.*195T=
NM_022464.5:c.*195T= MANE Select NP_071909.1:n.*195T=
NM_001037633.2:c.*195T= NP_001032722.1:n.*195T=