Canonical Allele Identifier: CA1950150439

Gene: SMPD1

Linked Data

• dbSNP Id: rs1848117079
• gnomAD v4: 11-6394788-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394788G>T , CM000673.2:g.6394788G>T	GRCh38
NC_000011.9:g.6416018G>T , CM000673.1:g.6416018G>T	GRCh37
NC_000011.8:g.6372594G>T	NCBI36
NG_011780.1:g.9364G>T
NG_029615.1:g.29627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*181G>T MANE Select	ENSP00000340409.4:n.*181G>T
ENST00000342245.8:c.*181G>T	ENSP00000340409.4:n.*181G>T
ENST00000526280.1:c.1134G>T
ENST00000533123.5:c.*804G>T	ENSP00000435950.1:n.*804G>T
ENST00000534405.5:c.*908G>T	ENSP00000434353.1:n.*908G>T
NM_000543.4:c.*181G>T	NP_000534.3:n.*181G>T
NM_001007593.2:c.*181G>T	NP_001007594.2:n.*181G>T
XM_011520303.1:c.*181G>T	XP_011518605.1:n.*181G>T
NM_001318087.1:c.*570G>T	NP_001305016.1:n.*570G>T
NM_001318088.1:c.*181G>T	NP_001305017.1:n.*181G>T
NM_001365135.1:c.*181G>T	NP_001352064.1:n.*181G>T
NR_027400.2:n.2090G>T
NR_134502.1:n.1629G>T
XR_001747940.2:n.2262G>T
XR_002957158.1:n.2444G>T
NM_000543.5:c.*181G>T MANE Select	NP_000534.3:n.*181G>T
NM_001007593.3:c.*181G>T	NP_001007594.2:n.*181G>T
NM_001318087.2:c.*570G>T	NP_001305016.1:n.*570G>T
NM_001318088.2:c.*181G>T	NP_001305017.1:n.*181G>T
NM_001365135.2:c.*181G>T	NP_001352064.1:n.*181G>T
NR_027400.3:n.2030G>T
NR_134502.2:n.1569G>T