Canonical Allele Identifier: CA1586135602

Gene: SIL1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139050982T= , CM000667.2:g.139050982T=	GRCh38
NC_000005.9:g.138386671T= , CM000667.1:g.138386671T=	GRCh37
NC_000005.8:g.138414570T=	NCBI36
NG_008112.1:g.152395A=
NG_008112.2:g.152395A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.309A= MANE Select	ENSP00000378294.2:p.Lys103=
ENST00000265195.9:c.309A=	ENSP00000265195.5:p.Lys103=
ENST00000394817.6:c.309A=	ENSP00000378294.2:p.Lys103=
ENST00000503732.1:n.136A=
ENST00000505830.5:c.339A=	ENSP00000426460.1:p.Lys113=
ENST00000507002.5:c.339A=	ENSP00000421890.1:p.Lys113=
ENST00000508639.5:c.309A=	ENSP00000427371.1:p.Lys103=
ENST00000509534.5:c.330A=	ENSP00000426858.1:p.Lys110=
ENST00000513453.5:c.309A=	ENSP00000424014.1:p.Lys103=
NM_001037633.1:c.309A=	NP_001032722.1:p.Lys103=
NM_022464.4:c.309A=	NP_071909.1:p.Lys103=
XM_011543570.1:c.339A=	XP_011541872.1:p.Lys113=
XM_011543570.2:c.339A=	XP_011541872.1:p.Lys113=
XM_024446164.1:c.309A=	XP_024301932.1:p.Lys103=
NM_022464.5:c.309A= MANE Select	NP_071909.1:p.Lys103=
NM_001037633.2:c.309A=	NP_001032722.1:p.Lys103=