Canonical Allele Identifier: CA1586077120

Gene: SIL1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947297_138947298delinsGC , CM000667.2:g.138947297_138947298delinsGC	GRCh38
NC_000005.9:g.138282986_138282987delinsGC , CM000667.1:g.138282986_138282987delinsGC	GRCh37
NC_000005.8:g.138310885_138310886delinsGC	NCBI36
NG_008112.1:g.256079_256080delinsGC
NG_008112.2:g.256079_256080delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1205_1206delinsGC MANE Select	ENSP00000378294.2:p.Gly402=
ENST00000265195.9:c.1205_1206delinsGC	ENSP00000265195.5:p.Gly402=
ENST00000394817.6:c.1205_1206delinsGC	ENSP00000378294.2:p.Gly402=
ENST00000509534.5:c.1226_1227delinsGC	ENSP00000426858.1:p.Gly409=
ENST00000515008.1:n.540_541delinsGC
NM_001037633.1:c.1205_1206delinsGC	NP_001032722.1:p.Gly402=
NM_022464.4:c.1205_1206delinsGC	NP_071909.1:p.Gly402=
XM_011543570.1:c.1235_1236delinsGC	XP_011541872.1:p.Gly412=
XM_011543570.2:c.1235_1236delinsGC	XP_011541872.1:p.Gly412=
XM_024446164.1:c.1205_1206delinsGC	XP_024301932.1:p.Gly402=
NM_022464.5:c.1205_1206delinsGC MANE Select	NP_071909.1:p.Gly402=
NM_001037633.2:c.1205_1206delinsGC	NP_001032722.1:p.Gly402=