Canonical Allele Identifier: CA361136540

Gene: SIL1

Linked Data

• ClinVar Variation Id: 906657
• ClinVar RCV Id: RCV001155990
• dbSNP Id: rs771297655
• gnomAD v4: 5-138947224-C-A
• MyVariant Identifiers: chr5:g.138282913C>A (hg19) ; chr5:g.138947224C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947224C>A , CM000667.2:g.138947224C>A	GRCh38
NC_000005.9:g.138282913C>A , CM000667.1:g.138282913C>A	GRCh37
NC_000005.8:g.138310812C>A	NCBI36
NG_008112.1:g.256153G>T
NG_008112.2:g.256153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1279G>T MANE Select	ENSP00000378294.2:p.Ala427Ser
ENST00000265195.9:c.1279G>T	ENSP00000265195.5:p.Ala427Ser
ENST00000394817.6:c.1279G>T	ENSP00000378294.2:p.Ala427Ser
ENST00000509534.5:c.1300G>T	ENSP00000426858.1:p.Ala434Ser
ENST00000515008.1:n.614G>T
NM_001037633.1:c.1279G>T	NP_001032722.1:p.Ala427Ser
NM_022464.4:c.1279G>T	NP_071909.1:p.Ala427Ser
XM_011543570.1:c.1309G>T	XP_011541872.1:p.Ala437Ser
XM_011543570.2:c.1309G>T	XP_011541872.1:p.Ala437Ser
XM_024446164.1:c.1279G>T	XP_024301932.1:p.Ala427Ser
NM_022464.5:c.1279G>T MANE Select	NP_071909.1:p.Ala427Ser
NM_001037633.2:c.1279G>T	NP_001032722.1:p.Ala427Ser