Canonical Allele Identifier: CA934767776

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392355_6392356insTTTTTTTTTTTTT , CM000673.2:g.6392355_6392356insTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.6413585_6413586insTTTTTTTTTTTTT , CM000673.1:g.6413585_6413586insTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.6370161_6370162insTTTTTTTTTTTTT	NCBI36
NG_011780.1:g.6931_6932insTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1091+199_1091+200insTTTTTTTTTTTTT MANE Select	ENSP00000340409.4:n.1091+199_1091+200insTTTTTTTTTTTTT
ENST00000342245.8:c.1091+199_1091+200insTTTTTTTTTTTTT	ENSP00000340409.4:n.1091+199_1091+200insTTTTTTTTTTTTT
ENST00000526280.1:c.320+159_320+160insTTTTTTTTTTTTT
ENST00000527275.5:c.1088+199_1088+200insTTTTTTTTTTTTT	ENSP00000435350.1:n.1088+199_1088+200insTTTTTTTTTTTTT
ENST00000531303.5:c.438+852_438+853insTTTTTTTTTTTTT	ENSP00000432625.1:n.438+852_438+853insTTTTTTTTTTTTT
ENST00000533123.5:c.1091+199_1091+200insTTTTTTTTTTTTT	ENSP00000435950.1:n.1091+199_1091+200insTTTTTTTTTTTTT
ENST00000534405.5:c.1131+159_1131+160insTTTTTTTTTTTTT	ENSP00000434353.1:n.1131+159_1131+160insTTTTTTTTTTTTT
NM_000543.4:c.1091+199_1091+200insTTTTTTTTTTTTT	NP_000534.3:n.1091+199_1091+200insTTTTTTTTTTTTT
NM_001007593.2:c.1088+199_1088+200insTTTTTTTTTTTTT	NP_001007594.2:n.1088+199_1088+200insTTTTTTTTTTTTT
XM_005253075.3:c.1091+199_1091+200insTTTTTTTTTTTTT	XP_005253132.1:n.1091+199_1091+200insTTTTTTTTTTTTT
XM_011520303.1:c.1131+159_1131+160insTTTTTTTTTTTTT	XP_011518605.1:n.1131+159_1131+160insTTTTTTTTTTTTT
XM_011520304.1:c.1131+159_1131+160insTTTTTTTTTTTTT	XP_011518606.1:n.1131+159_1131+160insTTTTTTTTTTTTT
XR_930886.1:n.1429+159_1429+160insTTTTTTTTTTTTT
NM_001318087.1:c.1091+199_1091+200insTTTTTTTTTTTTT	NP_001305016.1:n.1091+199_1091+200insTTTTTTTTTTTTT
NM_001318088.1:c.170+159_170+160insTTTTTTTTTTTTT	NP_001305017.1:n.170+159_170+160insTTTTTTTTTTTTT
NM_001365135.1:c.1131+159_1131+160insTTTTTTTTTTTTT	NP_001352064.1:n.1131+159_1131+160insTTTTTTTTTTTTT
NR_027400.2:n.1276+199_1276+200insTTTTTTTTTTTTT
NR_134502.1:n.623+852_623+853insTTTTTTTTTTTTT
XM_011520304.2:c.1131+159_1131+160insTTTTTTTTTTTTT	XP_011518606.1:n.1131+159_1131+160insTTTTTTTTTTTTT
XR_001747940.2:n.1256+159_1256+160insTTTTTTTTTTTTT
XR_002957158.1:n.1256+159_1256+160insTTTTTTTTTTTTT
NM_000543.5:c.1091+199_1091+200insTTTTTTTTTTTTT MANE Select	NP_000534.3:n.1091+199_1091+200insTTTTTTTTTTTTT
NM_001007593.3:c.1088+199_1088+200insTTTTTTTTTTTTT	NP_001007594.2:n.1088+199_1088+200insTTTTTTTTTTTTT
NM_001318087.2:c.1091+199_1091+200insTTTTTTTTTTTTT	NP_001305016.1:n.1091+199_1091+200insTTTTTTTTTTTTT
NM_001318088.2:c.170+159_170+160insTTTTTTTTTTTTT	NP_001305017.1:n.170+159_170+160insTTTTTTTTTTTTT
NM_001365135.2:c.1131+159_1131+160insTTTTTTTTTTTTT	NP_001352064.1:n.1131+159_1131+160insTTTTTTTTTTTTT
NR_027400.3:n.1216+199_1216+200insTTTTTTTTTTTTT
NR_134502.2:n.563+852_563+853insTTTTTTTTTTTTT