Canonical Allele Identifier: CA1434851379

Gene: STX18

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4524576C= , CM000666.2:g.4524576C=	GRCh38
NC_000004.11:g.4526303C= , CM000666.1:g.4526303C=	GRCh37
NC_000004.10:g.4577204C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306200.7:c.168+17221G= MANE Select	ENSP00000305810.2:n.168+17221G=
ENST00000306200.6:c.168+17221G=	ENSP00000305810.2:n.168+17221G=
ENST00000505286.5:c.168+17221G=	ENSP00000426648.1:n.168+17221G=
ENST00000507908.5:c.-76+17584G=	ENSP00000422376.1:n.-76+17584G=
ENST00000512780.2:n.235+17221G=
NM_016930.2:c.168+17221G=	NP_058626.1:n.168+17221G=
XM_011513479.1:c.168+17221G=	XP_011511781.1:n.168+17221G=
XM_011513480.1:c.168+17221G=	XP_011511782.1:n.168+17221G=
XM_011513481.1:c.168+17221G=	XP_011511783.1:n.168+17221G=
XM_011513482.1:c.168+17221G=	XP_011511784.1:n.168+17221G=
XM_011513483.1:c.168+17221G=	XP_011511785.1:n.168+17221G=
XM_011513485.1:c.-76+17584G=	XP_011511787.1:n.-76+17584G=
XR_924956.1:n.231+17221G=
XR_924957.1:n.231+17221G=
XR_924958.1:n.231+17221G=
NM_001346281.1:c.168+17221G=	NP_001333210.1:n.168+17221G=
NM_001346282.1:c.-76+17584G=	NP_001333211.1:n.-76+17584G=
NM_016930.3:c.168+17221G=	NP_058626.1:n.168+17221G=
NR_144414.1:n.270+17221G=
XM_017008296.1:c.168+17221G=	XP_016863785.1:n.168+17221G=
XM_017008298.1:c.168+17221G=	XP_016863787.1:n.168+17221G=
XR_001741239.1:n.231+17221G=
XR_001741564.1:n.3867G=
NM_016930.4:c.168+17221G= MANE Select	NP_058626.1:n.168+17221G=
NM_001346281.2:c.168+17221G=	NP_001333210.1:n.168+17221G=
NM_001346282.2:c.-76+17584G=	NP_001333211.1:n.-76+17584G=
NR_144414.2:n.252+17221G=