Canonical Allele Identifier: CA1950146376
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391885A= , CM000673.2:g.6391885A= GRCh38
NC_000011.9:g.6413115A= , CM000673.1:g.6413115A= GRCh37
NC_000011.8:g.6369691A= NCBI36
NG_011780.1:g.6461A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.820A= MANE Select ENSP00000340409.4:p.Met274=
ENST00000342245.8:c.820A= ENSP00000340409.4:p.Met274=
ENST00000526280.1:c.9A=
ENST00000527275.5:c.817A= ENSP00000435350.1:p.Met273=
ENST00000530395.1:c.1A= ENSP00000431479.1:p.Met1=
ENST00000531303.5:c.438+382A= ENSP00000432625.1:n.438+382A=
ENST00000533123.5:c.820A= ENSP00000435950.1:p.Met274=
ENST00000533196.1:n.375-121A=
ENST00000534405.5:c.820A= ENSP00000434353.1:p.Met274=
NM_000543.4:c.820A= NP_000534.3:p.Met274=
NM_001007593.2:c.817A= NP_001007594.2:p.Met273=
XM_005253075.3:c.820A= XP_005253132.1:p.Met274=
XM_011520303.1:c.820A= XP_011518605.1:p.Met274=
XM_011520304.1:c.820A= XP_011518606.1:p.Met274=
XR_930886.1:n.1118A=
NM_001318087.1:c.820A= NP_001305016.1:p.Met274=
NM_001318088.1:c.-142A= NP_001305017.1:n.-142A=
NM_001365135.1:c.820A= NP_001352064.1:p.Met274=
NR_027400.2:n.1005A=
NR_134502.1:n.623+382A=
XM_011520304.2:c.820A= XP_011518606.1:p.Met274=
XR_001747940.2:n.945A=
XR_002957158.1:n.945A=
NM_000543.5:c.820A= MANE Select NP_000534.3:p.Met274=
NM_001007593.3:c.817A= NP_001007594.2:p.Met273=
NM_001318087.2:c.820A= NP_001305016.1:p.Met274=
NM_001318088.2:c.-142A= NP_001305017.1:n.-142A=
NM_001365135.2:c.820A= NP_001352064.1:p.Met274=
NR_027400.3:n.945A=
NR_134502.2:n.563+382A=