Canonical Allele Identifier: CA7298755

Gene: SPATA7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88437542G>C , CM000676.2:g.88437542G>C	GRCh38
NC_000014.8:g.88903886G>C , CM000676.1:g.88903886G>C	GRCh37
NC_000014.7:g.87973639G>C	NCBI36
NG_021183.1:g.56899G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018418.5:c.1161-1G>C MANE Select	NP_060888.2:n.1161-1G>C
ENST00000393545.9:c.1161-1G>C MANE Select	ENSP00000377176.4:n.1161-1G>C
NM_001040428.3:c.1065-1G>C	NP_001035518.1:n.1065-1G>C
NM_001040428.4:c.1065-1G>C	NP_001035518.1:n.1065-1G>C
NM_018418.4:c.1161-1G>C	NP_060888.2:n.1161-1G>C
ENST00000045347.11:c.1161-1G>C	ENSP00000045347.7:n.1161-1G>C
ENST00000356583.9:c.1065-1G>C	ENSP00000348991.5:n.1065-1G>C
ENST00000393545.8:c.1161-1G>C	ENSP00000377176.4:n.1161-1G>C
ENST00000553303.1:n.591-1G>C
ENST00000553626.5:n.2940-1G>C
ENST00000554802.1:c.57-1G>C	ENSP00000451019.1:n.57-1G>C
ENST00000556406.5:c.134-1G>C
ENST00000556553.5:c.1065-1G>C	ENSP00000451128.1:n.1065-1G>C
ENST00000556666.5:n.1708-1G>C
XM_005267851.1:c.1164-1G>C	XP_005267908.1:n.1164-1G>C
XM_005267852.1:c.1068-1G>C	XP_005267909.1:n.1068-1G>C
XM_005267852.2:c.1068-1G>C	XP_005267909.1:n.1068-1G>C
XM_005267854.1:c.972-1G>C	XP_005267911.1:n.972-1G>C
XM_005267855.1:c.972-1G>C	XP_005267912.1:n.972-1G>C
XM_006720204.1:c.1164-1G>C	XP_006720267.1:n.1164-1G>C
XM_006720205.1:c.1164-1G>C	XP_006720268.1:n.1164-1G>C
XM_011536951.1:c.1011-1G>C	XP_011535253.1:n.1011-1G>C
XM_011536952.1:c.993-1G>C	XP_011535254.1:n.993-1G>C
XM_011536953.1:c.846-1G>C	XP_011535255.1:n.846-1G>C
XM_017021452.1:c.1008-1G>C	XP_016876941.1:n.1008-1G>C
XM_017021453.1:c.972-1G>C	XP_016876942.1:n.972-1G>C
XM_017021454.1:c.969-1G>C	XP_016876943.1:n.969-1G>C
XM_017021455.1:c.969-1G>C	XP_016876944.1:n.969-1G>C
XM_017021456.1:c.969-1G>C	XP_016876945.1:n.969-1G>C
XM_017021457.1:c.843-1G>C	XP_016876946.1:n.843-1G>C
XM_024449660.1:c.990-1G>C	XP_024305428.1:n.990-1G>C
XR_002957563.1:n.1342-1G>C