Canonical Allele Identifier: CA1950147089

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392515_6392517delinsTGA , CM000673.2:g.6392515_6392517delinsTGA	GRCh38
NC_000011.9:g.6413745_6413747delinsTGA , CM000673.1:g.6413745_6413747delinsTGA	GRCh37
NC_000011.8:g.6370321_6370323delinsTGA	NCBI36
NG_011780.1:g.7091_7093delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1091+359_1091+361delinsTGA MANE Select	ENSP00000340409.4:n.1091+359_1091+361delinsTGA
ENST00000342245.8:c.1091+359_1091+361delinsTGA	ENSP00000340409.4:n.1091+359_1091+361delinsTGA
ENST00000526280.1:c.320+319_320+321delinsTGA
ENST00000527275.5:c.1088+359_1088+361delinsTGA	ENSP00000435350.1:n.1088+359_1088+361delinsTGA
ENST00000531303.5:c.439-701_439-699delinsTGA	ENSP00000432625.1:n.439-701_439-699delinsTGA
ENST00000533123.5:c.1091+359_1091+361delinsTGA	ENSP00000435950.1:n.1091+359_1091+361delinsTGA
ENST00000534405.5:c.1131+319_1131+321delinsTGA	ENSP00000434353.1:n.1131+319_1131+321delinsTGA
NM_000543.4:c.1091+359_1091+361delinsTGA	NP_000534.3:n.1091+359_1091+361delinsTGA
NM_001007593.2:c.1088+359_1088+361delinsTGA	NP_001007594.2:n.1088+359_1088+361delinsTGA
XM_005253075.3:c.1091+359_1091+361delinsTGA	XP_005253132.1:n.1091+359_1091+361delinsTGA
XM_011520303.1:c.1131+319_1131+321delinsTGA	XP_011518605.1:n.1131+319_1131+321delinsTGA
XM_011520304.1:c.1131+319_1131+321delinsTGA	XP_011518606.1:n.1131+319_1131+321delinsTGA
XR_930886.1:n.1429+319_1429+321delinsTGA
NM_001318087.1:c.1091+359_1091+361delinsTGA	NP_001305016.1:n.1091+359_1091+361delinsTGA
NM_001318088.1:c.170+319_170+321delinsTGA	NP_001305017.1:n.170+319_170+321delinsTGA
NM_001365135.1:c.1131+319_1131+321delinsTGA	NP_001352064.1:n.1131+319_1131+321delinsTGA
NR_027400.2:n.1276+359_1276+361delinsTGA
NR_134502.1:n.624-701_624-699delinsTGA
XM_011520304.2:c.1131+319_1131+321delinsTGA	XP_011518606.1:n.1131+319_1131+321delinsTGA
XR_001747940.2:n.1256+319_1256+321delinsTGA
XR_002957158.1:n.1256+319_1256+321delinsTGA
NM_000543.5:c.1091+359_1091+361delinsTGA MANE Select	NP_000534.3:n.1091+359_1091+361delinsTGA
NM_001007593.3:c.1088+359_1088+361delinsTGA	NP_001007594.2:n.1088+359_1088+361delinsTGA
NM_001318087.2:c.1091+359_1091+361delinsTGA	NP_001305016.1:n.1091+359_1091+361delinsTGA
NM_001318088.2:c.170+319_170+321delinsTGA	NP_001305017.1:n.170+319_170+321delinsTGA
NM_001365135.2:c.1131+319_1131+321delinsTGA	NP_001352064.1:n.1131+319_1131+321delinsTGA
NR_027400.3:n.1216+359_1216+361delinsTGA
NR_134502.2:n.564-701_564-699delinsTGA