Canonical Allele Identifier: CA1950148256
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393481G= , CM000673.2:g.6393481G= GRCh38
NC_000011.9:g.6414711G= , CM000673.1:g.6414711G= GRCh37
NC_000011.8:g.6371287G= NCBI36
NG_011780.1:g.8057G=
NG_029615.1:g.30934C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1263+94G= MANE Select ENSP00000340409.4:n.1263+94G=
ENST00000342245.8:c.1263+94G= ENSP00000340409.4:n.1263+94G=
ENST00000526280.1:c.321-136G=
ENST00000527275.5:c.1260+94G= ENSP00000435350.1:n.1260+94G=
ENST00000531303.5:c.*94+94G= ENSP00000432625.1:n.*94+94G=
ENST00000531336.1:n.95+94G=
ENST00000533123.5:c.1092-136G= ENSP00000435950.1:n.1092-136G=
ENST00000534405.5:c.*94+94G= ENSP00000434353.1:n.*94+94G=
NM_000543.4:c.1263+94G= NP_000534.3:n.1263+94G=
NM_001007593.2:c.1260+94G= NP_001007594.2:n.1260+94G=
XM_005253075.3:c.1263+94G= XP_005253132.1:n.1263+94G=
XM_011520303.1:c.1132-136G= XP_011518605.1:n.1132-136G=
XM_011520304.1:c.1132-136G= XP_011518606.1:n.1132-136G=
XR_930886.1:n.1601+94G=
NM_001318087.1:c.1263+94G= NP_001305016.1:n.1263+94G=
NM_001318088.1:c.342+94G= NP_001305017.1:n.342+94G=
NM_001365135.1:c.1132-136G= NP_001352064.1:n.1132-136G=
NR_027400.2:n.1277-136G=
NR_134502.1:n.795+94G=
XM_011520304.2:c.1132-136G= XP_011518606.1:n.1132-136G=
XR_001747940.2:n.1428+94G=
XR_002957158.1:n.1428+94G=
NM_000543.5:c.1263+94G= MANE Select NP_000534.3:n.1263+94G=
NM_001007593.3:c.1260+94G= NP_001007594.2:n.1260+94G=
NM_001318087.2:c.1263+94G= NP_001305016.1:n.1263+94G=
NM_001318088.2:c.342+94G= NP_001305017.1:n.342+94G=
NM_001365135.2:c.1132-136G= NP_001352064.1:n.1132-136G=
NR_027400.3:n.1217-136G=
NR_134502.2:n.735+94G=