Canonical Allele Identifier: CA206585

Gene: SYT14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210094554_210094556del , CM000663.2:g.210094554_210094556del	GRCh38
NC_000001.10:g.210267899_210267901del , CM000663.1:g.210267899_210267901del	GRCh37
NC_000001.9:g.208334522_208334524del	NCBI36
NG_031962.1:g.161381_161383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367019.6:c.675_677del MANE Select	ENSP00000355986.1:p.Glu225del
ENST00000699295.1:c.1545_1547del	ENSP00000514275.1:p.Glu515del
ENST00000637265.1:c.1545_1547del	ENSP00000489897.1:p.Glu515del
ENST00000637945.1:c.*535_*537del	ENSP00000489671.1:n.*535_*537del
ENST00000367015.5:c.561_563del	ENSP00000355982.1:p.Glu187del
ENST00000367019.5:c.675_677del	ENSP00000355986.1:p.Glu225del
ENST00000399639.6:c.561_563del	ENSP00000445837.2:p.Glu187del
ENST00000472886.5:c.675_677del	ENSP00000418901.1:p.Glu225del
ENST00000534859.2:c.442_444del
ENST00000537238.5:c.561_563del	ENSP00000437423.1:p.Glu187del
ENST00000629778.2:c.810_812del	ENSP00000486230.1:p.Glu270del
NM_001146261.2:c.810_812del	NP_001139733.1:p.Glu270del
NM_001146262.2:c.675_677del	NP_001139734.1:p.Glu225del
NM_001146264.2:c.810_812del	NP_001139736.1:p.Glu270del
NM_001256006.1:c.561_563del	NP_001242935.1:p.Glu187del
NM_153262.3:c.675_677del	NP_694994.2:p.Glu225del
NR_027459.2:n.971_973del
XM_006711262.2:c.1545_1547del	XP_006711325.1:p.Glu515del
XM_011509388.1:c.1545_1547del	XP_011507690.1:p.Glu515del
XM_011509389.1:c.1545_1547del	XP_011507691.1:p.Glu515del
XM_006711262.3:c.1545_1547del	XP_006711325.1:p.Glu515del
XM_017000931.1:c.1545_1547del	XP_016856420.1:p.Glu515del
XM_017000932.2:c.561_563del	XP_016856421.1:p.Glu187del
XM_017000933.2:c.561_563del	XP_016856422.1:p.Glu187del
XM_017000934.2:c.561_563del	XP_016856423.1:p.Glu187del
XM_017000935.2:c.7-5458_7-5456del	XP_016856424.1:n.7-5458_7-5456del
NM_001146262.3:c.675_677del	NP_001139734.1:p.Glu225del
NM_001146264.3:c.810_812del	NP_001139736.1:p.Glu270del
NM_153262.4:c.675_677del	NP_694994.2:p.Glu225del
NR_027459.3:n.928_930del
NM_001146261.3:c.810_812del	NP_001139733.1:p.Glu270del
NM_001256006.2:c.561_563del	NP_001242935.1:p.Glu187del
NM_001146261.4:c.810_812del	NP_001139733.1:p.Glu270del
NM_001146262.4:c.675_677del MANE Select	NP_001139734.1:p.Glu225del
NM_001146264.4:c.810_812del	NP_001139736.1:p.Glu270del
NM_001256006.3:c.561_563del	NP_001242935.1:p.Glu187del
NM_001397544.1:c.1545_1547del	NP_001384473.1:p.Glu515del
NM_001397545.1:c.1545_1547del	NP_001384474.1:p.Glu515del
NM_153262.5:c.675_677del	NP_694994.2:p.Glu225del