Canonical Allele Identifier: CA2612220896

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6390487-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390487C>T , CM000673.2:g.6390487C>T	GRCh38
NC_000011.9:g.6411717C>T , CM000673.1:g.6411717C>T	GRCh37
NC_000011.8:g.6368293C>T	NCBI36
NG_011780.1:g.5063C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.-112C>T MANE Select	ENSP00000340409.4:n.-112C>T
ENST00000342245.8:c.-112C>T	ENSP00000340409.4:n.-112C>T
ENST00000527275.5:c.-112C>T	ENSP00000435350.1:n.-112C>T
ENST00000530395.1:c.-248C>T	ENSP00000431479.1:n.-248C>T
ENST00000533196.1:n.48C>T
ENST00000534405.5:c.-112C>T	ENSP00000434353.1:n.-112C>T
NM_000543.4:c.-112C>T	NP_000534.3:n.-112C>T
NM_001007593.2:c.-112C>T	NP_001007594.2:n.-112C>T
XM_005253075.3:c.-112C>T	XP_005253132.1:n.-112C>T
XM_011520303.1:c.-112C>T	XP_011518605.1:n.-112C>T
XM_011520304.1:c.-112C>T	XP_011518606.1:n.-112C>T
XR_930886.1:n.187C>T
NM_001318087.1:c.-112C>T	NP_001305016.1:n.-112C>T
NM_001318088.1:c.-1073C>T	NP_001305017.1:n.-1073C>T
NM_001365135.1:c.-112C>T	NP_001352064.1:n.-112C>T
NR_027400.2:n.74C>T
NR_134502.1:n.74C>T
XM_011520304.2:c.-112C>T	XP_011518606.1:n.-112C>T
XR_001747940.2:n.14C>T
XR_002957158.1:n.14C>T
NM_000543.5:c.-112C>T MANE Select	NP_000534.3:n.-112C>T
NM_001007593.3:c.-112C>T	NP_001007594.2:n.-112C>T
NM_001318087.2:c.-112C>T	NP_001305016.1:n.-112C>T
NM_001318088.2:c.-1073C>T	NP_001305017.1:n.-1073C>T
NM_001365135.2:c.-112C>T	NP_001352064.1:n.-112C>T
NR_027400.3:n.14C>T
NR_134502.2:n.14C>T