Canonical Allele Identifier: CA1586100146
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947037C= , CM000667.2:g.138947037C= GRCh38
NC_000005.9:g.138282726C= , CM000667.1:g.138282726C= GRCh37
NC_000005.8:g.138310625C= NCBI36
NG_008112.1:g.256340G=
NG_008112.2:g.256340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*80G= MANE Select ENSP00000378294.2:n.*80G=
ENST00000265195.9:c.*80G= ENSP00000265195.5:n.*80G=
ENST00000394817.6:c.*80G= ENSP00000378294.2:n.*80G=
ENST00000509534.5:c.*80G= ENSP00000426858.1:n.*80G=
ENST00000515008.1:n.801G=
NM_001037633.1:c.*80G= NP_001032722.1:n.*80G=
NM_022464.4:c.*80G= NP_071909.1:n.*80G=
XM_011543570.1:c.*80G= XP_011541872.1:n.*80G=
XM_011543570.2:c.*80G= XP_011541872.1:n.*80G=
XM_024446164.1:c.*80G= XP_024301932.1:n.*80G=
NM_022464.5:c.*80G= MANE Select NP_071909.1:n.*80G=
NM_001037633.2:c.*80G= NP_001032722.1:n.*80G=