Canonical Allele Identifier: CA128236066

Gene: SIL1

Linked Data

• ClinVar Variation Id: 906655
• ClinVar RCV Id: RCV001155987
• dbSNP Id: rs981026347
• gnomAD v3: 5-138947012-G-A
• gnomAD v4: 5-138947012-G-A
• MyVariant Identifiers: chr5:g.138282701G>A (hg19) ; chr5:g.138947012G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947012G>A , CM000667.2:g.138947012G>A	GRCh38
NC_000005.9:g.138282701G>A , CM000667.1:g.138282701G>A	GRCh37
NC_000005.8:g.138310600G>A	NCBI36
NG_008112.1:g.256365C>T
NG_008112.2:g.256365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.*105C>T MANE Select	ENSP00000378294.2:n.*105C>T
ENST00000265195.9:c.*105C>T	ENSP00000265195.5:n.*105C>T
ENST00000394817.6:c.*105C>T	ENSP00000378294.2:n.*105C>T
ENST00000515008.1:n.826C>T
NM_001037633.1:c.*105C>T	NP_001032722.1:n.*105C>T
NM_022464.4:c.*105C>T	NP_071909.1:n.*105C>T
XM_011543570.1:c.*105C>T	XP_011541872.1:n.*105C>T
XM_011543570.2:c.*105C>T	XP_011541872.1:n.*105C>T
XM_024446164.1:c.*105C>T	XP_024301932.1:n.*105C>T
NM_022464.5:c.*105C>T MANE Select	NP_071909.1:n.*105C>T
NM_001037633.2:c.*105C>T	NP_001032722.1:n.*105C>T