Canonical Allele Identifier: CA3432418
Community Standard Title: NM_022464.5(SIL1):c.1005G>A (p.Leu335=)
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138951195C>T , CM000667.2:g.138951195C>T GRCh38
NC_000005.9:g.138286884C>T , CM000667.1:g.138286884C>T GRCh37
NC_000005.8:g.138314783C>T NCBI36
NG_008112.1:g.252182G>A
NG_008112.2:g.252182G>A

Transcript Alleles

HGVS Amino-acid Change
NM_022464.5:c.1005G>A MANE Select NP_071909.1:p.Leu335=
ENST00000394817.7:c.1005G>A MANE Select ENSP00000378294.2:p.Leu335=
NM_001037633.1:c.1005G>A NP_001032722.1:p.Leu335=
NM_001037633.2:c.1005G>A NP_001032722.1:p.Leu335=
NM_022464.4:c.1005G>A NP_071909.1:p.Leu335=
ENST00000265195.9:c.1005G>A ENSP00000265195.5:p.Leu335=
ENST00000394817.6:c.1005G>A ENSP00000378294.2:p.Leu335=
ENST00000509534.5:c.1026G>A ENSP00000426858.1:p.Leu342=
ENST00000515008.1:n.340G>A
XM_011543570.1:c.1035G>A XP_011541872.1:p.Leu345=
XM_011543570.2:c.1035G>A XP_011541872.1:p.Leu345=
XM_024446164.1:c.1005G>A XP_024301932.1:p.Leu335=