Canonical Allele Identifier: CA16618119

Gene: SIL1

Linked Data

• ClinVar Variation Id: 424547
• ClinVar RCV Id: RCV000481013
• dbSNP Id: rs1064797034
• MyVariant Identifiers: chr5:g.138282999A>G (hg19) ; chr5:g.138947310A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947310A>G , CM000667.2:g.138947310A>G	GRCh38
NC_000005.9:g.138282999A>G , CM000667.1:g.138282999A>G	GRCh37
NC_000005.8:g.138310898A>G	NCBI36
NG_008112.1:g.256067T>C
NG_008112.2:g.256067T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1193T>C MANE Select	ENSP00000378294.2:p.Leu398Pro
ENST00000265195.9:c.1193T>C	ENSP00000265195.5:p.Leu398Pro
ENST00000394817.6:c.1193T>C	ENSP00000378294.2:p.Leu398Pro
ENST00000509534.5:c.1214T>C	ENSP00000426858.1:p.Leu405Pro
ENST00000515008.1:n.528T>C
NM_001037633.1:c.1193T>C	NP_001032722.1:p.Leu398Pro
NM_022464.4:c.1193T>C	NP_071909.1:p.Leu398Pro
XM_011543570.1:c.1223T>C	XP_011541872.1:p.Leu408Pro
XM_011543570.2:c.1223T>C	XP_011541872.1:p.Leu408Pro
XM_024446164.1:c.1193T>C	XP_024301932.1:p.Leu398Pro
NM_022464.5:c.1193T>C MANE Select	NP_071909.1:p.Leu398Pro
NM_001037633.2:c.1193T>C	NP_001032722.1:p.Leu398Pro