Canonical Allele Identifier: CA361136551

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282918A>T (hg19) ; chr5:g.138947229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947229A>T , CM000667.2:g.138947229A>T	GRCh38
NC_000005.9:g.138282918A>T , CM000667.1:g.138282918A>T	GRCh37
NC_000005.8:g.138310817A>T	NCBI36
NG_008112.1:g.256148T>A
NG_008112.2:g.256148T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1274T>A MANE Select	ENSP00000378294.2:p.Leu425Gln
ENST00000265195.9:c.1274T>A	ENSP00000265195.5:p.Leu425Gln
ENST00000394817.6:c.1274T>A	ENSP00000378294.2:p.Leu425Gln
ENST00000509534.5:c.1295T>A	ENSP00000426858.1:p.Leu432Gln
ENST00000515008.1:n.609T>A
NM_001037633.1:c.1274T>A	NP_001032722.1:p.Leu425Gln
NM_022464.4:c.1274T>A	NP_071909.1:p.Leu425Gln
XM_011543570.1:c.1304T>A	XP_011541872.1:p.Leu435Gln
XM_011543570.2:c.1304T>A	XP_011541872.1:p.Leu435Gln
XM_024446164.1:c.1274T>A	XP_024301932.1:p.Leu425Gln
NM_022464.5:c.1274T>A MANE Select	NP_071909.1:p.Leu425Gln
NM_001037633.2:c.1274T>A	NP_001032722.1:p.Leu425Gln