Canonical Allele Identifier: CA934768263
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392495_6392515dup , CM000673.2:g.6392495_6392515dup GRCh38
NC_000011.9:g.6413725_6413745dup , CM000673.1:g.6413725_6413745dup GRCh37
NC_000011.8:g.6370301_6370321dup NCBI36
NG_011780.1:g.7071_7091dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1091+339_1091+359dup MANE Select ENSP00000340409.4:n.1091+339_1091+359dup
ENST00000342245.8:c.1091+339_1091+359dup ENSP00000340409.4:n.1091+339_1091+359dup
ENST00000526280.1:c.320+299_320+319dup
ENST00000527275.5:c.1088+339_1088+359dup ENSP00000435350.1:n.1088+339_1088+359dup
ENST00000531303.5:c.439-721_439-701dup ENSP00000432625.1:n.439-721_439-701dup
ENST00000533123.5:c.1091+339_1091+359dup ENSP00000435950.1:n.1091+339_1091+359dup
ENST00000534405.5:c.1131+299_1131+319dup ENSP00000434353.1:n.1131+299_1131+319dup
NM_000543.4:c.1091+339_1091+359dup NP_000534.3:n.1091+339_1091+359dup
NM_001007593.2:c.1088+339_1088+359dup NP_001007594.2:n.1088+339_1088+359dup
XM_005253075.3:c.1091+339_1091+359dup XP_005253132.1:n.1091+339_1091+359dup
XM_011520303.1:c.1131+299_1131+319dup XP_011518605.1:n.1131+299_1131+319dup
XM_011520304.1:c.1131+299_1131+319dup XP_011518606.1:n.1131+299_1131+319dup
XR_930886.1:n.1429+299_1429+319dup
NM_001318087.1:c.1091+339_1091+359dup NP_001305016.1:n.1091+339_1091+359dup
NM_001318088.1:c.170+299_170+319dup NP_001305017.1:n.170+299_170+319dup
NM_001365135.1:c.1131+299_1131+319dup NP_001352064.1:n.1131+299_1131+319dup
NR_027400.2:n.1276+339_1276+359dup
NR_134502.1:n.624-721_624-701dup
XM_011520304.2:c.1131+299_1131+319dup XP_011518606.1:n.1131+299_1131+319dup
XR_001747940.2:n.1256+299_1256+319dup
XR_002957158.1:n.1256+299_1256+319dup
NM_000543.5:c.1091+339_1091+359dup MANE Select NP_000534.3:n.1091+339_1091+359dup
NM_001007593.3:c.1088+339_1088+359dup NP_001007594.2:n.1088+339_1088+359dup
NM_001318087.2:c.1091+339_1091+359dup NP_001305016.1:n.1091+339_1091+359dup
NM_001318088.2:c.170+299_170+319dup NP_001305017.1:n.170+299_170+319dup
NM_001365135.2:c.1131+299_1131+319dup NP_001352064.1:n.1131+299_1131+319dup
NR_027400.3:n.1216+339_1216+359dup
NR_134502.2:n.564-721_564-701dup