Canonical Allele Identifier: CA1950149229
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6394116G= , CM000673.2:g.6394116G= GRCh38
NC_000011.9:g.6415346G= , CM000673.1:g.6415346G= GRCh37
NC_000011.8:g.6371922G= NCBI36
NG_011780.1:g.8692G=
NG_029615.1:g.30299C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1486+75G= MANE Select ENSP00000340409.4:n.1486+75G=
ENST00000342245.8:c.1486+75G= ENSP00000340409.4:n.1486+75G=
ENST00000526280.1:c.543+75G=
ENST00000527275.5:c.1483+75G= ENSP00000435350.1:n.1483+75G=
ENST00000531303.5:c.*318-62G= ENSP00000432625.1:n.*318-62G=
ENST00000531336.1:n.393G=
ENST00000532367.1:n.397G=
ENST00000533123.5:c.*213+75G= ENSP00000435950.1:n.*213+75G=
ENST00000534405.5:c.*317+75G= ENSP00000434353.1:n.*317+75G=
NM_000543.4:c.1486+75G= NP_000534.3:n.1486+75G=
NM_001007593.2:c.1483+75G= NP_001007594.2:n.1483+75G=
XM_005253075.3:c.1487-62G= XP_005253132.1:n.1487-62G=
XM_011520303.1:c.1354+75G= XP_011518605.1:n.1354+75G=
XM_011520304.1:c.1355-62G= XP_011518606.1:n.1355-62G=
NM_001318087.1:c.1487-62G= NP_001305016.1:n.1487-62G=
NM_001318088.1:c.565+75G= NP_001305017.1:n.565+75G=
NM_001365135.1:c.1354+75G= NP_001352064.1:n.1354+75G=
NR_027400.2:n.1499+75G=
NR_134502.1:n.1019-62G=
XM_011520304.2:c.1355-62G= XP_011518606.1:n.1355-62G=
XR_001747940.2:n.1652-62G=
XR_002957158.1:n.1853+75G=
NM_000543.5:c.1486+75G= MANE Select NP_000534.3:n.1486+75G=
NM_001007593.3:c.1483+75G= NP_001007594.2:n.1483+75G=
NM_001318087.2:c.1487-62G= NP_001305016.1:n.1487-62G=
NM_001318088.2:c.565+75G= NP_001305017.1:n.565+75G=
NM_001365135.2:c.1354+75G= NP_001352064.1:n.1354+75G=
NR_027400.3:n.1439+75G=
NR_134502.2:n.959-62G=