Canonical Allele Identifier: CA361136681

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282985C>A (hg19) ; chr5:g.138947296C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947296C>A , CM000667.2:g.138947296C>A	GRCh38
NC_000005.9:g.138282985C>A , CM000667.1:g.138282985C>A	GRCh37
NC_000005.8:g.138310884C>A	NCBI36
NG_008112.1:g.256081G>T
NG_008112.2:g.256081G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1207G>T MANE Select	ENSP00000378294.2:p.Val403Phe
ENST00000265195.9:c.1207G>T	ENSP00000265195.5:p.Val403Phe
ENST00000394817.6:c.1207G>T	ENSP00000378294.2:p.Val403Phe
ENST00000509534.5:c.1228G>T	ENSP00000426858.1:p.Val410Phe
ENST00000515008.1:n.542G>T
NM_001037633.1:c.1207G>T	NP_001032722.1:p.Val403Phe
NM_022464.4:c.1207G>T	NP_071909.1:p.Val403Phe
XM_011543570.1:c.1237G>T	XP_011541872.1:p.Val413Phe
XM_011543570.2:c.1237G>T	XP_011541872.1:p.Val413Phe
XM_024446164.1:c.1207G>T	XP_024301932.1:p.Val403Phe
NM_022464.5:c.1207G>T MANE Select	NP_071909.1:p.Val403Phe
NM_001037633.2:c.1207G>T	NP_001032722.1:p.Val403Phe