Canonical Allele Identifier: CA1417400345

Gene: SI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046904T= , CM000665.2:g.165046904T=	GRCh38
NC_000003.11:g.164764692T= , CM000665.1:g.164764692T=	GRCh37
NC_000003.10:g.166247386T=	NCBI36
NG_017043.1:g.36592A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264382.8:c.1824A= MANE Select	ENSP00000264382.3:p.Ser608=
ENST00000264382.7:c.1824A=	ENSP00000264382.3:p.Ser608=
NM_001041.3:c.1824A=	NP_001032.2:p.Ser608=
XM_011513078.1:c.1725A=	XP_011511380.1:p.Ser575=
XM_011513078.2:c.1725A=	XP_011511380.1:p.Ser575=
NM_001041.4:c.1824A= MANE Select	NP_001032.2:p.Ser608=