Canonical Allele Identifier: CA1586100008
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946757C= , CM000667.2:g.138946757C= GRCh38
NC_000005.9:g.138282446C= , CM000667.1:g.138282446C= GRCh37
NC_000005.8:g.138310345C= NCBI36
NG_008112.1:g.256620G=
NG_008112.2:g.256620G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*360G= MANE Select ENSP00000378294.2:n.*360G=
ENST00000265195.9:c.*360G= ENSP00000265195.5:n.*360G=
ENST00000394817.6:c.*360G= ENSP00000378294.2:n.*360G=
NM_001037633.1:c.*360G= NP_001032722.1:n.*360G=
NM_022464.4:c.*360G= NP_071909.1:n.*360G=
XM_011543570.2:c.*360G= XP_011541872.1:n.*360G=
XM_024446164.1:c.*360G= XP_024301932.1:n.*360G=
NM_022464.5:c.*360G= MANE Select NP_071909.1:n.*360G=
NM_001037633.2:c.*360G= NP_001032722.1:n.*360G=