Canonical Allele Identifier: CA361136567

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282927A>C (hg19) ; chr5:g.138947238A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947238A>C , CM000667.2:g.138947238A>C	GRCh38
NC_000005.9:g.138282927A>C , CM000667.1:g.138282927A>C	GRCh37
NC_000005.8:g.138310826A>C	NCBI36
NG_008112.1:g.256139T>G
NG_008112.2:g.256139T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1265T>G MANE Select	ENSP00000378294.2:p.Leu422Arg
ENST00000265195.9:c.1265T>G	ENSP00000265195.5:p.Leu422Arg
ENST00000394817.6:c.1265T>G	ENSP00000378294.2:p.Leu422Arg
ENST00000509534.5:c.1286T>G	ENSP00000426858.1:p.Leu429Arg
ENST00000515008.1:n.600T>G
NM_001037633.1:c.1265T>G	NP_001032722.1:p.Leu422Arg
NM_022464.4:c.1265T>G	NP_071909.1:p.Leu422Arg
XM_011543570.1:c.1295T>G	XP_011541872.1:p.Leu432Arg
XM_011543570.2:c.1295T>G	XP_011541872.1:p.Leu432Arg
XM_024446164.1:c.1265T>G	XP_024301932.1:p.Leu422Arg
NM_022464.5:c.1265T>G MANE Select	NP_071909.1:p.Leu422Arg
NM_001037633.2:c.1265T>G	NP_001032722.1:p.Leu422Arg