Canonical Allele Identifier: CA361136683

Gene: SIL1

Linked Data

• dbSNP Id: rs1050490804
• MyVariant Identifiers: chr5:g.138282987C>A (hg19) ; chr5:g.138947298C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947298C>A , CM000667.2:g.138947298C>A	GRCh38
NC_000005.9:g.138282987C>A , CM000667.1:g.138282987C>A	GRCh37
NC_000005.8:g.138310886C>A	NCBI36
NG_008112.1:g.256079G>T
NG_008112.2:g.256079G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1205G>T MANE Select	ENSP00000378294.2:p.Gly402Val
ENST00000265195.9:c.1205G>T	ENSP00000265195.5:p.Gly402Val
ENST00000394817.6:c.1205G>T	ENSP00000378294.2:p.Gly402Val
ENST00000509534.5:c.1226G>T	ENSP00000426858.1:p.Gly409Val
ENST00000515008.1:n.540G>T
NM_001037633.1:c.1205G>T	NP_001032722.1:p.Gly402Val
NM_022464.4:c.1205G>T	NP_071909.1:p.Gly402Val
XM_011543570.1:c.1235G>T	XP_011541872.1:p.Gly412Val
XM_011543570.2:c.1235G>T	XP_011541872.1:p.Gly412Val
XM_024446164.1:c.1205G>T	XP_024301932.1:p.Gly402Val
NM_022464.5:c.1205G>T MANE Select	NP_071909.1:p.Gly402Val
NM_001037633.2:c.1205G>T	NP_001032722.1:p.Gly402Val