Canonical Allele Identifier: CA361136678

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282984A>C (hg19) ; chr5:g.138947295A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947295A>C , CM000667.2:g.138947295A>C	GRCh38
NC_000005.9:g.138282984A>C , CM000667.1:g.138282984A>C	GRCh37
NC_000005.8:g.138310883A>C	NCBI36
NG_008112.1:g.256082T>G
NG_008112.2:g.256082T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1208T>G MANE Select	ENSP00000378294.2:p.Val403Gly
ENST00000265195.9:c.1208T>G	ENSP00000265195.5:p.Val403Gly
ENST00000394817.6:c.1208T>G	ENSP00000378294.2:p.Val403Gly
ENST00000509534.5:c.1229T>G	ENSP00000426858.1:p.Val410Gly
ENST00000515008.1:n.543T>G
NM_001037633.1:c.1208T>G	NP_001032722.1:p.Val403Gly
NM_022464.4:c.1208T>G	NP_071909.1:p.Val403Gly
XM_011543570.1:c.1238T>G	XP_011541872.1:p.Val413Gly
XM_011543570.2:c.1238T>G	XP_011541872.1:p.Val413Gly
XM_024446164.1:c.1208T>G	XP_024301932.1:p.Val403Gly
NM_022464.5:c.1208T>G MANE Select	NP_071909.1:p.Val403Gly
NM_001037633.2:c.1208T>G	NP_001032722.1:p.Val403Gly