Canonical Allele Identifier: CA1969344390

Gene: SPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47354897G= , CM000673.2:g.47354897G=	GRCh38
NC_000011.9:g.47376448G= , CM000673.1:g.47376448G=	GRCh37
NC_000011.8:g.47333024G=	NCBI36
NG_007667.1:g.2806C= , LRG_386:g.2806C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713542.1:c.*587C=	ENSP00000518838.1:n.*587C=
ENST00000713543.1:c.*330C=	ENSP00000518839.1:n.*330C=
ENST00000378538.8:c.*330C= MANE Select	ENSP00000367799.4:n.*330C=
ENST00000378538.7:c.*330C=	ENSP00000367799.3:n.*330C=
NM_001080547.1:c.*330C=	NP_001074016.1:n.*330C=
NM_003120.2:c.*330C=	NP_003111.2:n.*330C=
XM_011520305.1:c.*330C=	XP_011518607.1:n.*330C=
XM_011520306.1:c.*330C=	XP_011518608.1:n.*330C=
XM_011520307.1:c.*330C=	XP_011518609.1:n.*330C=
XM_011520308.1:c.*330C=	XP_011518610.1:n.*330C=
XM_017018173.1:c.*330C=	XP_016873662.1:n.*330C=
NM_001080547.2:c.*330C=	NP_001074016.1:n.*330C=
NM_003120.3:c.*330C= MANE Select	NP_003111.2:n.*330C=