Canonical Allele Identifier: CA379368903
Gene: SMPD1 HGNC NCBI

Linked Data

gnomAD v4: 11-6391504-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391504G>T , CM000673.2:g.6391504G>T GRCh38
NC_000011.9:g.6412734G>T , CM000673.1:g.6412734G>T GRCh37
NC_000011.8:g.6369310G>T NCBI36
NG_011780.1:g.6080G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.439G>T MANE Select ENSP00000340409.4:p.Val147Leu
ENST00000342245.8:c.439G>T ENSP00000340409.4:p.Val147Leu
ENST00000527275.5:c.436G>T ENSP00000435350.1:p.Val146Leu
ENST00000530395.1:c.-95-286G>T ENSP00000431479.1:n.-95-286G>T
ENST00000531303.5:c.438+1G>T ENSP00000432625.1:n.438+1G>T
ENST00000533123.5:c.439G>T ENSP00000435950.1:p.Val147Leu
ENST00000533196.1:n.375-502G>T
ENST00000534405.5:c.439G>T ENSP00000434353.1:p.Val147Leu
NM_000543.4:c.439G>T NP_000534.3:p.Val147Leu
NM_001007593.2:c.436G>T NP_001007594.2:p.Val146Leu
XM_005253075.3:c.439G>T XP_005253132.1:p.Val147Leu
XM_011520303.1:c.439G>T XP_011518605.1:p.Val147Leu
XM_011520304.1:c.439G>T XP_011518606.1:p.Val147Leu
XR_930886.1:n.737G>T
NM_001318087.1:c.439G>T NP_001305016.1:p.Val147Leu
NM_001318088.1:c.-523G>T NP_001305017.1:n.-523G>T
NM_001365135.1:c.439G>T NP_001352064.1:p.Val147Leu
NR_027400.2:n.624G>T
NR_134502.1:n.623+1G>T
XM_011520304.2:c.439G>T XP_011518606.1:p.Val147Leu
XR_001747940.2:n.564G>T
XR_002957158.1:n.564G>T
NM_000543.5:c.439G>T MANE Select NP_000534.3:p.Val147Leu
NM_001007593.3:c.436G>T NP_001007594.2:p.Val146Leu
NM_001318087.2:c.439G>T NP_001305016.1:p.Val147Leu
NM_001318088.2:c.-523G>T NP_001305017.1:n.-523G>T
NM_001365135.2:c.439G>T NP_001352064.1:p.Val147Leu
NR_027400.3:n.564G>T
NR_134502.2:n.563+1G>T