Canonical Allele Identifier: CA355052067

Gene: SI

Linked Data

• MyVariant Identifiers: chr3:g.164764641A>T (hg19) ; chr3:g.165046853A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046853A>T , CM000665.2:g.165046853A>T	GRCh38
NC_000003.11:g.164764641A>T , CM000665.1:g.164764641A>T	GRCh37
NC_000003.10:g.166247335A>T	NCBI36
NG_017043.1:g.36643T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264382.8:c.1875T>A MANE Select	ENSP00000264382.3:p.Phe625Leu
ENST00000264382.7:c.1875T>A	ENSP00000264382.3:p.Phe625Leu
NM_001041.3:c.1875T>A	NP_001032.2:p.Phe625Leu
XM_011513078.1:c.1776T>A	XP_011511380.1:p.Phe592Leu
XM_011513078.2:c.1776T>A	XP_011511380.1:p.Phe592Leu
NM_001041.4:c.1875T>A MANE Select	NP_001032.2:p.Phe625Leu