Canonical Allele Identifier: CA2675501547
Gene: SIL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138946951C>A , CM000667.2:g.138946951C>A GRCh38
NC_000005.9:g.138282640C>A , CM000667.1:g.138282640C>A GRCh37
NC_000005.8:g.138310539C>A NCBI36
NG_008112.1:g.256426G>T
NG_008112.2:g.256426G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394817.7:c.*166G>T MANE Select ENSP00000378294.2:n.*166G>T
ENST00000265195.9:c.*166G>T ENSP00000265195.5:n.*166G>T
ENST00000394817.6:c.*166G>T ENSP00000378294.2:n.*166G>T
NM_001037633.1:c.*166G>T NP_001032722.1:n.*166G>T
NM_022464.4:c.*166G>T NP_071909.1:n.*166G>T
XM_011543570.2:c.*166G>T XP_011541872.1:n.*166G>T
XM_024446164.1:c.*166G>T XP_024301932.1:n.*166G>T
NM_022464.5:c.*166G>T MANE Select NP_071909.1:n.*166G>T
NM_001037633.2:c.*166G>T NP_001032722.1:n.*166G>T