Canonical Allele Identifier: CA1586099998
Gene: SIL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946730A= , CM000667.2:g.138946730A= GRCh38
NC_000005.9:g.138282419A= , CM000667.1:g.138282419A= GRCh37
NC_000005.8:g.138310318A= NCBI36
NG_008112.1:g.256647T=
NG_008112.2:g.256647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*387T= MANE Select ENSP00000378294.2:n.*387T=
ENST00000394817.6:c.*387T= ENSP00000378294.2:n.*387T=
NM_001037633.1:c.*387T= NP_001032722.1:n.*387T=
NM_022464.4:c.*387T= NP_071909.1:n.*387T=
XM_011543570.2:c.*387T= XP_011541872.1:n.*387T=
XM_024446164.1:c.*387T= XP_024301932.1:n.*387T=
NM_022464.5:c.*387T= MANE Select NP_071909.1:n.*387T=
NM_001037633.2:c.*387T= NP_001032722.1:n.*387T=
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