Canonical Allele Identifier: CA2156475260

Gene: SYNE3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95476110A= , CM000676.2:g.95476110A=	GRCh38
NC_000014.8:g.95942447A= , CM000676.1:g.95942447A=	GRCh37
NC_000014.7:g.95012200A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682763.1:c.-14-275T= MANE Select	ENSP00000507501.1:n.-14-275T=
XM_005267376.3:c.176-275T=	XP_005267433.2:n.176-275T=
XM_005267377.2:c.-14-275T=	XP_005267434.1:n.-14-275T=
XM_006720063.2:c.-14-275T=	XP_006720126.1:n.-14-275T=
XM_011536513.1:c.176-275T=	XP_011534815.1:n.176-275T=
XM_011536514.1:c.176-275T=	XP_011534816.1:n.176-275T=
XM_011536515.1:c.11-275T=	XP_011534817.1:n.11-275T=
XM_011536516.1:c.176-275T=	XP_011534818.1:n.176-275T=
XM_005267377.4:c.-14-275T=	XP_005267434.1:n.-14-275T=
XM_006720063.4:c.-14-275T=	XP_006720126.1:n.-14-275T=
XM_011536515.3:c.11-275T=	XP_011534817.1:n.11-275T=
XM_017021057.1:c.-14-275T=	XP_016876546.1:n.-14-275T=
NM_001363692.2:c.-14-275T=	NP_001350621.1:n.-14-275T=
NM_001384281.1:c.-14-275T=	NP_001371210.1:n.-14-275T=
NM_001384282.1:c.-14-275T=	NP_001371211.1:n.-14-275T=
NM_001384283.1:c.11-275T=	NP_001371212.1:n.11-275T=
NM_001384284.1:c.-14-275T=	NP_001371213.1:n.-14-275T=
NM_152592.6:c.-14-275T= MANE Select	NP_689805.3:n.-14-275T=