Canonical Allele Identifier: CA361136684
Gene: SIL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947298C>G , CM000667.2:g.138947298C>G GRCh38
NC_000005.9:g.138282987C>G , CM000667.1:g.138282987C>G GRCh37
NC_000005.8:g.138310886C>G NCBI36
NG_008112.1:g.256079G>C
NG_008112.2:g.256079G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.1205G>C MANE Select ENSP00000378294.2:p.Gly402Ala
ENST00000265195.9:c.1205G>C ENSP00000265195.5:p.Gly402Ala
ENST00000394817.6:c.1205G>C ENSP00000378294.2:p.Gly402Ala
ENST00000509534.5:c.1226G>C ENSP00000426858.1:p.Gly409Ala
ENST00000515008.1:n.540G>C
NM_001037633.1:c.1205G>C NP_001032722.1:p.Gly402Ala
NM_022464.4:c.1205G>C NP_071909.1:p.Gly402Ala
XM_011543570.1:c.1235G>C XP_011541872.1:p.Gly412Ala
XM_011543570.2:c.1235G>C XP_011541872.1:p.Gly412Ala
XM_024446164.1:c.1205G>C XP_024301932.1:p.Gly402Ala
NM_022464.5:c.1205G>C MANE Select NP_071909.1:p.Gly402Ala
NM_001037633.2:c.1205G>C NP_001032722.1:p.Gly402Ala