Canonical Allele Identifier: CA1586100195
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947145A= , CM000667.2:g.138947145A= GRCh38
NC_000005.9:g.138282834A= , CM000667.1:g.138282834A= GRCh37
NC_000005.8:g.138310733A= NCBI36
NG_008112.1:g.256232T=
NG_008112.2:g.256232T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.1358T= MANE Select ENSP00000378294.2:p.Val453=
ENST00000265195.9:c.1358T= ENSP00000265195.5:p.Val453=
ENST00000394817.6:c.1358T= ENSP00000378294.2:p.Val453=
ENST00000509534.5:c.1379T= ENSP00000426858.1:p.Val460=
ENST00000515008.1:n.693T=
NM_001037633.1:c.1358T= NP_001032722.1:p.Val453=
NM_022464.4:c.1358T= NP_071909.1:p.Val453=
XM_011543570.1:c.1388T= XP_011541872.1:p.Val463=
XM_011543570.2:c.1388T= XP_011541872.1:p.Val463=
XM_024446164.1:c.1358T= XP_024301932.1:p.Val453=
NM_022464.5:c.1358T= MANE Select NP_071909.1:p.Val453=
NM_001037633.2:c.1358T= NP_001032722.1:p.Val453=