Canonical Allele Identifier: CA2768602000
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946803C>T , CM000667.2:g.138946803C>T GRCh38
NC_000005.9:g.138282492C>T , CM000667.1:g.138282492C>T GRCh37
NC_000005.8:g.138310391C>T NCBI36
NG_008112.1:g.256574G>A
NG_008112.2:g.256574G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*314G>A MANE Select ENSP00000378294.2:n.*314G>A
ENST00000265195.9:c.*314G>A ENSP00000265195.5:n.*314G>A
ENST00000394817.6:c.*314G>A ENSP00000378294.2:n.*314G>A
NM_001037633.1:c.*314G>A NP_001032722.1:n.*314G>A
NM_022464.4:c.*314G>A NP_071909.1:n.*314G>A
XM_011543570.2:c.*314G>A XP_011541872.1:n.*314G>A
XM_024446164.1:c.*314G>A XP_024301932.1:n.*314G>A
NM_022464.5:c.*314G>A MANE Select NP_071909.1:n.*314G>A
NM_001037633.2:c.*314G>A NP_001032722.1:n.*314G>A