Canonical Allele Identifier: CA2675501365
Gene: SIL1 HGNC NCBI

Linked Data

gnomAD v4: 5-138946780-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946780C>T , CM000667.2:g.138946780C>T GRCh38
NC_000005.9:g.138282469C>T , CM000667.1:g.138282469C>T GRCh37
NC_000005.8:g.138310368C>T NCBI36
NG_008112.1:g.256597G>A
NG_008112.2:g.256597G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*337G>A MANE Select ENSP00000378294.2:n.*337G>A
ENST00000265195.9:c.*337G>A ENSP00000265195.5:n.*337G>A
ENST00000394817.6:c.*337G>A ENSP00000378294.2:n.*337G>A
NM_001037633.1:c.*337G>A NP_001032722.1:n.*337G>A
NM_022464.4:c.*337G>A NP_071909.1:n.*337G>A
XM_011543570.2:c.*337G>A XP_011541872.1:n.*337G>A
XM_024446164.1:c.*337G>A XP_024301932.1:n.*337G>A
NM_022464.5:c.*337G>A MANE Select NP_071909.1:n.*337G>A
NM_001037633.2:c.*337G>A NP_001032722.1:n.*337G>A
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