Canonical Allele Identifier: CA1586100150

Gene: SIL1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947048_138947049delinsAG , CM000667.2:g.138947048_138947049delinsAG	GRCh38
NC_000005.9:g.138282737_138282738delinsAG , CM000667.1:g.138282737_138282738delinsAG	GRCh37
NC_000005.8:g.138310636_138310637delinsAG	NCBI36
NG_008112.1:g.256328_256329delinsCT
NG_008112.2:g.256328_256329delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.*68_*69delinsCT MANE Select	ENSP00000378294.2:n.*68_*69delinsCT
ENST00000265195.9:c.*68_*69delinsCT	ENSP00000265195.5:n.*68_*69delinsCT
ENST00000394817.6:c.*68_*69delinsCT	ENSP00000378294.2:n.*68_*69delinsCT
ENST00000509534.5:c.*68_*69delinsCT	ENSP00000426858.1:n.*68_*69delinsCT
ENST00000515008.1:n.789_790delinsCT
NM_001037633.1:c.*68_*69delinsCT	NP_001032722.1:n.*68_*69delinsCT
NM_022464.4:c.*68_*69delinsCT	NP_071909.1:n.*68_*69delinsCT
XM_011543570.1:c.*68_*69delinsCT	XP_011541872.1:n.*68_*69delinsCT
XM_011543570.2:c.*68_*69delinsCT	XP_011541872.1:n.*68_*69delinsCT
XM_024446164.1:c.*68_*69delinsCT	XP_024301932.1:n.*68_*69delinsCT
NM_022464.5:c.*68_*69delinsCT MANE Select	NP_071909.1:n.*68_*69delinsCT
NM_001037633.2:c.*68_*69delinsCT	NP_001032722.1:n.*68_*69delinsCT