Canonical Allele Identifier: CA361136548

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282916G>C (hg19) ; chr5:g.138947227G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947227G>C , CM000667.2:g.138947227G>C	GRCh38
NC_000005.9:g.138282916G>C , CM000667.1:g.138282916G>C	GRCh37
NC_000005.8:g.138310815G>C	NCBI36
NG_008112.1:g.256150C>G
NG_008112.2:g.256150C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1276C>G MANE Select	ENSP00000378294.2:p.Gln426Glu
ENST00000265195.9:c.1276C>G	ENSP00000265195.5:p.Gln426Glu
ENST00000394817.6:c.1276C>G	ENSP00000378294.2:p.Gln426Glu
ENST00000509534.5:c.1297C>G	ENSP00000426858.1:p.Gln433Glu
ENST00000515008.1:n.611C>G
NM_001037633.1:c.1276C>G	NP_001032722.1:p.Gln426Glu
NM_022464.4:c.1276C>G	NP_071909.1:p.Gln426Glu
XM_011543570.1:c.1306C>G	XP_011541872.1:p.Gln436Glu
XM_011543570.2:c.1306C>G	XP_011541872.1:p.Gln436Glu
XM_024446164.1:c.1276C>G	XP_024301932.1:p.Gln426Glu
NM_022464.5:c.1276C>G MANE Select	NP_071909.1:p.Gln426Glu
NM_001037633.2:c.1276C>G	NP_001032722.1:p.Gln426Glu