Canonical Allele Identifier: CA1586100157
Gene: SIL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138947062G= , CM000667.2:g.138947062G= GRCh38
NC_000005.9:g.138282751G= , CM000667.1:g.138282751G= GRCh37
NC_000005.8:g.138310650G= NCBI36
NG_008112.1:g.256315C=
NG_008112.2:g.256315C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*55C= MANE Select ENSP00000378294.2:n.*55C=
ENST00000265195.9:c.*55C= ENSP00000265195.5:n.*55C=
ENST00000394817.6:c.*55C= ENSP00000378294.2:n.*55C=
ENST00000509534.5:c.*55C= ENSP00000426858.1:n.*55C=
ENST00000515008.1:n.776C=
NM_001037633.1:c.*55C= NP_001032722.1:n.*55C=
NM_022464.4:c.*55C= NP_071909.1:n.*55C=
XM_011543570.1:c.*55C= XP_011541872.1:n.*55C=
XM_011543570.2:c.*55C= XP_011541872.1:n.*55C=
XM_024446164.1:c.*55C= XP_024301932.1:n.*55C=
NM_022464.5:c.*55C= MANE Select NP_071909.1:n.*55C=
NM_001037633.2:c.*55C= NP_001032722.1:n.*55C=