Canonical Allele Identifier: CA2675501634
Gene: SIL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947046T>C , CM000667.2:g.138947046T>C GRCh38
NC_000005.9:g.138282735T>C , CM000667.1:g.138282735T>C GRCh37
NC_000005.8:g.138310634T>C NCBI36
NG_008112.1:g.256331A>G
NG_008112.2:g.256331A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394817.7:c.*71A>G MANE Select ENSP00000378294.2:n.*71A>G
ENST00000265195.9:c.*71A>G ENSP00000265195.5:n.*71A>G
ENST00000394817.6:c.*71A>G ENSP00000378294.2:n.*71A>G
ENST00000509534.5:c.*71A>G ENSP00000426858.1:n.*71A>G
ENST00000515008.1:n.792A>G
NM_001037633.1:c.*71A>G NP_001032722.1:n.*71A>G
NM_022464.4:c.*71A>G NP_071909.1:n.*71A>G
XM_011543570.1:c.*71A>G XP_011541872.1:n.*71A>G
XM_011543570.2:c.*71A>G XP_011541872.1:n.*71A>G
XM_024446164.1:c.*71A>G XP_024301932.1:n.*71A>G
NM_022464.5:c.*71A>G MANE Select NP_071909.1:n.*71A>G
NM_001037633.2:c.*71A>G NP_001032722.1:n.*71A>G