Canonical Allele Identifier: CA2153574890

Gene: SPATA7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88396042G= , CM000676.2:g.88396042G=	GRCh38
NC_000014.8:g.88862386G= , CM000676.1:g.88862386G=	GRCh37
NC_000014.7:g.87932139G=	NCBI36
NG_021183.1:g.15399G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393545.9:c.191-114G= MANE Select	ENSP00000377176.4:n.191-114G=
ENST00000045347.11:c.191-114G=	ENSP00000045347.7:n.191-114G=
ENST00000356583.9:c.95-114G=	ENSP00000348991.5:n.95-114G=
ENST00000393545.8:c.191-114G=	ENSP00000377176.4:n.191-114G=
ENST00000553626.5:n.319-114G=
ENST00000553885.5:c.95-114G=	ENSP00000450606.1:n.95-114G=
ENST00000553908.5:c.95-114G=	ENSP00000452546.1:n.95-114G=
ENST00000554102.5:n.334-114G=
ENST00000554168.5:c.*148-114G=	ENSP00000451663.1:n.*148-114G=
ENST00000555356.5:c.*148-114G=	ENSP00000450654.1:n.*148-114G=
ENST00000555401.5:c.20-114G=	ENSP00000452435.1:n.20-114G=
ENST00000555515.5:c.191-114G=	ENSP00000450882.1:n.191-114G=
ENST00000555534.5:c.191-114G=	ENSP00000450515.1:n.191-114G=
ENST00000555715.5:c.*223-114G=	ENSP00000451181.1:n.*223-114G=
ENST00000556553.5:c.95-114G=	ENSP00000451128.1:n.95-114G=
ENST00000556870.5:c.95-114G=	ENSP00000452359.1:n.95-114G=
ENST00000557248.5:c.191-114G=	ENSP00000451690.1:n.191-114G=
ENST00000557724.5:c.*244-114G=	ENSP00000452364.1:n.*244-114G=
NM_001040428.3:c.95-114G=	NP_001035518.1:n.95-114G=
NM_018418.4:c.191-114G=	NP_060888.2:n.191-114G=
XM_005267851.1:c.191-114G=	XP_005267908.1:n.191-114G=
XM_005267852.1:c.95-114G=	XP_005267909.1:n.95-114G=
XM_005267854.1:c.-64-114G=	XP_005267911.1:n.-64-114G=
XM_005267855.1:c.-64-114G=	XP_005267912.1:n.-64-114G=
XM_006720204.1:c.191-114G=	XP_006720267.1:n.191-114G=
XM_006720205.1:c.191-114G=	XP_006720268.1:n.191-114G=
XM_011536951.1:c.38-114G=	XP_011535253.1:n.38-114G=
XM_011536952.1:c.20-114G=	XP_011535254.1:n.20-114G=
XM_011536953.1:c.-128-114G=	XP_011535255.1:n.-128-114G=
XM_005267852.2:c.95-114G=	XP_005267909.1:n.95-114G=
XM_017021452.1:c.38-114G=	XP_016876941.1:n.38-114G=
XM_017021453.1:c.-64-114G=	XP_016876942.1:n.-64-114G=
XM_017021454.1:c.-64-114G=	XP_016876943.1:n.-64-114G=
XM_017021455.1:c.-64-114G=	XP_016876944.1:n.-64-114G=
XM_017021456.1:c.-64-114G=	XP_016876945.1:n.-64-114G=
XM_017021457.1:c.-128-114G=	XP_016876946.1:n.-128-114G=
XM_024449660.1:c.20-114G=	XP_024305428.1:n.20-114G=
XR_002957563.1:n.262-114G=
NM_018418.5:c.191-114G= MANE Select	NP_060888.2:n.191-114G=
NM_001040428.4:c.95-114G=	NP_001035518.1:n.95-114G=