Canonical Allele Identifier: CA1586100227
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947222A= , CM000667.2:g.138947222A= GRCh38
NC_000005.9:g.138282911A= , CM000667.1:g.138282911A= GRCh37
NC_000005.8:g.138310810A= NCBI36
NG_008112.1:g.256155T=
NG_008112.2:g.256155T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.1281T= MANE Select ENSP00000378294.2:p.Ala427=
ENST00000265195.9:c.1281T= ENSP00000265195.5:p.Ala427=
ENST00000394817.6:c.1281T= ENSP00000378294.2:p.Ala427=
ENST00000509534.5:c.1302T= ENSP00000426858.1:p.Ala434=
ENST00000515008.1:n.616T=
NM_001037633.1:c.1281T= NP_001032722.1:p.Ala427=
NM_022464.4:c.1281T= NP_071909.1:p.Ala427=
XM_011543570.1:c.1311T= XP_011541872.1:p.Ala437=
XM_011543570.2:c.1311T= XP_011541872.1:p.Ala437=
XM_024446164.1:c.1281T= XP_024301932.1:p.Ala427=
NM_022464.5:c.1281T= MANE Select NP_071909.1:p.Ala427=
NM_001037633.2:c.1281T= NP_001032722.1:p.Ala427=