Canonical Allele Identifier: CA1586100048
Gene: SIL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946843T= , CM000667.2:g.138946843T= GRCh38
NC_000005.9:g.138282532T= , CM000667.1:g.138282532T= GRCh37
NC_000005.8:g.138310431T= NCBI36
NG_008112.1:g.256534A=
NG_008112.2:g.256534A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*274A= MANE Select ENSP00000378294.2:n.*274A=
ENST00000265195.9:c.*274A= ENSP00000265195.5:n.*274A=
ENST00000394817.6:c.*274A= ENSP00000378294.2:n.*274A=
NM_001037633.1:c.*274A= NP_001032722.1:n.*274A=
NM_022464.4:c.*274A= NP_071909.1:n.*274A=
XM_011543570.2:c.*274A= XP_011541872.1:n.*274A=
XM_024446164.1:c.*274A= XP_024301932.1:n.*274A=
NM_022464.5:c.*274A= MANE Select NP_071909.1:n.*274A=
NM_001037633.2:c.*274A= NP_001032722.1:n.*274A=
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