Canonical Allele Identifier: CA361136579
Gene: SIL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947243C>A , CM000667.2:g.138947243C>A GRCh38
NC_000005.9:g.138282932C>A , CM000667.1:g.138282932C>A GRCh37
NC_000005.8:g.138310831C>A NCBI36
NG_008112.1:g.256134G>T
NG_008112.2:g.256134G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.1260G>T MANE Select ENSP00000378294.2:p.Arg420Ser
ENST00000265195.9:c.1260G>T ENSP00000265195.5:p.Arg420Ser
ENST00000394817.6:c.1260G>T ENSP00000378294.2:p.Arg420Ser
ENST00000509534.5:c.1281G>T ENSP00000426858.1:p.Arg427Ser
ENST00000515008.1:n.595G>T
NM_001037633.1:c.1260G>T NP_001032722.1:p.Arg420Ser
NM_022464.4:c.1260G>T NP_071909.1:p.Arg420Ser
XM_011543570.1:c.1290G>T XP_011541872.1:p.Arg430Ser
XM_011543570.2:c.1290G>T XP_011541872.1:p.Arg430Ser
XM_024446164.1:c.1260G>T XP_024301932.1:p.Arg420Ser
NM_022464.5:c.1260G>T MANE Select NP_071909.1:p.Arg420Ser
NM_001037633.2:c.1260G>T NP_001032722.1:p.Arg420Ser