Canonical Allele Identifier: CA379376327
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6394285A>T , CM000673.2:g.6394285A>T GRCh38
NC_000011.9:g.6415515A>T , CM000673.1:g.6415515A>T GRCh37
NC_000011.8:g.6372091A>T NCBI36
NG_011780.1:g.8861A>T
NG_029615.1:g.30130T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1574A>T MANE Select ENSP00000340409.4:p.Gln525Leu
ENST00000342245.8:c.1574A>T ENSP00000340409.4:p.Gln525Leu
ENST00000526280.1:c.631A>T
ENST00000527275.5:c.1571A>T ENSP00000435350.1:p.Gln524Leu
ENST00000531303.5:c.*425A>T ENSP00000432625.1:n.*425A>T
ENST00000531336.1:n.562A>T
ENST00000533123.5:c.*301A>T ENSP00000435950.1:n.*301A>T
ENST00000534405.5:c.*405A>T ENSP00000434353.1:n.*405A>T
NM_000543.4:c.1574A>T NP_000534.3:p.Gln525Leu
NM_001007593.2:c.1571A>T NP_001007594.2:p.Gln524Leu
XM_005253075.3:c.*67A>T XP_005253132.1:n.*67A>T
XM_011520303.1:c.1442A>T XP_011518605.1:p.Gln481Leu
XM_011520304.1:c.*67A>T XP_011518606.1:n.*67A>T
NM_001318087.1:c.*67A>T NP_001305016.1:n.*67A>T
NM_001318088.1:c.653A>T NP_001305017.1:p.Gln218Leu
NM_001365135.1:c.1442A>T NP_001352064.1:p.Gln481Leu
NR_027400.2:n.1587A>T
NR_134502.1:n.1126A>T
XM_011520304.2:c.*67A>T XP_011518606.1:n.*67A>T
XR_001747940.2:n.1759A>T
XR_002957158.1:n.1941A>T
NM_000543.5:c.1574A>T MANE Select NP_000534.3:p.Gln525Leu
NM_001007593.3:c.1571A>T NP_001007594.2:p.Gln524Leu
NM_001318087.2:c.*67A>T NP_001305016.1:n.*67A>T
NM_001318088.2:c.653A>T NP_001305017.1:p.Gln218Leu
NM_001365135.2:c.1442A>T NP_001352064.1:p.Gln481Leu
NR_027400.3:n.1527A>T
NR_134502.2:n.1066A>T