Canonical Allele Identifier: CA1586100059
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946869T= , CM000667.2:g.138946869T= GRCh38
NC_000005.9:g.138282558T= , CM000667.1:g.138282558T= GRCh37
NC_000005.8:g.138310457T= NCBI36
NG_008112.1:g.256508A=
NG_008112.2:g.256508A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*248A= MANE Select ENSP00000378294.2:n.*248A=
ENST00000265195.9:c.*248A= ENSP00000265195.5:n.*248A=
ENST00000394817.6:c.*248A= ENSP00000378294.2:n.*248A=
NM_001037633.1:c.*248A= NP_001032722.1:n.*248A=
NM_022464.4:c.*248A= NP_071909.1:n.*248A=
XM_011543570.2:c.*248A= XP_011541872.1:n.*248A=
XM_024446164.1:c.*248A= XP_024301932.1:n.*248A=
NM_022464.5:c.*248A= MANE Select NP_071909.1:n.*248A=
NM_001037633.2:c.*248A= NP_001032722.1:n.*248A=