Canonical Allele Identifier: CA128236294

Gene: SIL1

Linked Data

• dbSNP Id: rs398124389
• gnomAD v2: 5-138282937-C-A
• gnomAD v3: 5-138947248-C-A
• gnomAD v4: 5-138947248-C-A
• MyVariant Identifiers: chr5:g.138282937C>A (hg19) ; chr5:g.138947248C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947248C>A , CM000667.2:g.138947248C>A	GRCh38
NC_000005.9:g.138282937C>A , CM000667.1:g.138282937C>A	GRCh37
NC_000005.8:g.138310836C>A	NCBI36
NG_008112.1:g.256129G>T
NG_008112.2:g.256129G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1255G>T MANE Select	ENSP00000378294.2:p.Gly419Cys
ENST00000265195.9:c.1255G>T	ENSP00000265195.5:p.Gly419Cys
ENST00000394817.6:c.1255G>T	ENSP00000378294.2:p.Gly419Cys
ENST00000509534.5:c.1276G>T	ENSP00000426858.1:p.Gly426Cys
ENST00000515008.1:n.590G>T
NM_001037633.1:c.1255G>T	NP_001032722.1:p.Gly419Cys
NM_022464.4:c.1255G>T	NP_071909.1:p.Gly419Cys
XM_011543570.1:c.1285G>T	XP_011541872.1:p.Gly429Cys
XM_011543570.2:c.1285G>T	XP_011541872.1:p.Gly429Cys
XM_024446164.1:c.1255G>T	XP_024301932.1:p.Gly419Cys
NM_022464.5:c.1255G>T MANE Select	NP_071909.1:p.Gly419Cys
NM_001037633.2:c.1255G>T	NP_001032722.1:p.Gly419Cys