Canonical Allele Identifier: CA15105361

Gene: SYT14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210155468G>T , CM000663.2:g.210155468G>T	GRCh38
NC_000001.10:g.210328813G>T , CM000663.1:g.210328813G>T	GRCh37
NC_000001.9:g.208395436G>T	NCBI36
NG_031962.1:g.222295G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001146262.4:c.1165-253G>T MANE Select	NP_001139734.1:n.1165-253G>T
ENST00000367019.6:c.1165-253G>T MANE Select	ENSP00000355986.1:n.1165-253G>T
NM_001146261.2:c.1300-253G>T	NP_001139733.1:n.1300-253G>T
NM_001146261.3:c.1300-253G>T	NP_001139733.1:n.1300-253G>T
NM_001146261.4:c.1300-253G>T	NP_001139733.1:n.1300-253G>T
NM_001146262.2:c.1165-253G>T	NP_001139734.1:n.1165-253G>T
NM_001146262.3:c.1165-253G>T	NP_001139734.1:n.1165-253G>T
NM_001146264.2:c.1300-253G>T	NP_001139736.1:n.1300-253G>T
NM_001146264.3:c.1300-253G>T	NP_001139736.1:n.1300-253G>T
NM_001146264.4:c.1300-253G>T	NP_001139736.1:n.1300-253G>T
NM_001256006.1:c.1051-253G>T	NP_001242935.1:n.1051-253G>T
NM_001256006.2:c.1051-253G>T	NP_001242935.1:n.1051-253G>T
NM_001256006.3:c.1051-253G>T	NP_001242935.1:n.1051-253G>T
NM_001397544.1:c.2035-253G>T	NP_001384473.1:n.2035-253G>T
NM_001397545.1:c.2035-253G>T	NP_001384474.1:n.2035-253G>T
NM_153262.3:c.1165-253G>T	NP_694994.2:n.1165-253G>T
NM_153262.4:c.1165-253G>T	NP_694994.2:n.1165-253G>T
NM_153262.5:c.1165-253G>T	NP_694994.2:n.1165-253G>T
NR_027459.2:n.1190-253G>T
NR_027459.3:n.1147-253G>T
ENST00000367015.5:c.1051-253G>T	ENSP00000355982.1:n.1051-253G>T
ENST00000367019.5:c.1165-253G>T	ENSP00000355986.1:n.1165-253G>T
ENST00000399639.6:c.780-253G>T	ENSP00000445837.2:n.780-253G>T
ENST00000472886.5:c.1165-253G>T	ENSP00000418901.1:n.1165-253G>T
ENST00000534859.2:c.932-253G>T
ENST00000537238.5:c.1051-253G>T	ENSP00000437423.1:n.1051-253G>T
ENST00000629778.2:c.1300-253G>T	ENSP00000486230.1:n.1300-253G>T
ENST00000637265.1:c.2035-253G>T	ENSP00000489897.1:n.2035-253G>T
ENST00000637945.1:c.*1025-253G>T	ENSP00000489671.1:n.*1025-253G>T
ENST00000699295.1:c.2035-253G>T	ENSP00000514275.1:n.2035-253G>T
XM_006711262.2:c.2035-253G>T	XP_006711325.1:n.2035-253G>T
XM_006711262.3:c.2035-253G>T	XP_006711325.1:n.2035-253G>T
XM_011509388.1:c.2035-253G>T	XP_011507690.1:n.2035-253G>T
XM_011509389.1:c.2035-253G>T	XP_011507691.1:n.2035-253G>T
XM_017000931.1:c.2035-253G>T	XP_016856420.1:n.2035-253G>T
XM_017000932.2:c.1051-253G>T	XP_016856421.1:n.1051-253G>T
XM_017000933.2:c.1051-253G>T	XP_016856422.1:n.1051-253G>T
XM_017000934.2:c.1051-253G>T	XP_016856423.1:n.1051-253G>T
XM_017000935.2:c.457-253G>T	XP_016856424.1:n.457-253G>T