Canonical Allele Identifier: CA1586100006
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946751T= , CM000667.2:g.138946751T= GRCh38
NC_000005.9:g.138282440T= , CM000667.1:g.138282440T= GRCh37
NC_000005.8:g.138310339T= NCBI36
NG_008112.1:g.256626A=
NG_008112.2:g.256626A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*366A= MANE Select ENSP00000378294.2:n.*366A=
ENST00000394817.6:c.*366A= ENSP00000378294.2:n.*366A=
NM_001037633.1:c.*366A= NP_001032722.1:n.*366A=
NM_022464.4:c.*366A= NP_071909.1:n.*366A=
XM_011543570.2:c.*366A= XP_011541872.1:n.*366A=
XM_024446164.1:c.*366A= XP_024301932.1:n.*366A=
NM_022464.5:c.*366A= MANE Select NP_071909.1:n.*366A=
NM_001037633.2:c.*366A= NP_001032722.1:n.*366A=