Canonical Allele Identifier: CA379371046

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6391870-G-T
• MyVariant Identifiers: chr11:g.6413100G>T (hg19) ; chr11:g.6391870G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391870G>T , CM000673.2:g.6391870G>T	GRCh38
NC_000011.9:g.6413100G>T , CM000673.1:g.6413100G>T	GRCh37
NC_000011.8:g.6369676G>T	NCBI36
NG_011780.1:g.6446G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.805G>T MANE Select	ENSP00000340409.4:p.Ala269Ser
ENST00000342245.8:c.805G>T	ENSP00000340409.4:p.Ala269Ser
ENST00000527275.5:c.802G>T	ENSP00000435350.1:p.Ala268Ser
ENST00000530395.1:c.-15G>T	ENSP00000431479.1:n.-15G>T
ENST00000531303.5:c.438+367G>T	ENSP00000432625.1:n.438+367G>T
ENST00000533123.5:c.805G>T	ENSP00000435950.1:p.Ala269Ser
ENST00000533196.1:n.375-136G>T
ENST00000534405.5:c.805G>T	ENSP00000434353.1:p.Ala269Ser
NM_000543.4:c.805G>T	NP_000534.3:p.Ala269Ser
NM_001007593.2:c.802G>T	NP_001007594.2:p.Ala268Ser
XM_005253075.3:c.805G>T	XP_005253132.1:p.Ala269Ser
XM_011520303.1:c.805G>T	XP_011518605.1:p.Ala269Ser
XM_011520304.1:c.805G>T	XP_011518606.1:p.Ala269Ser
XR_930886.1:n.1103G>T
NM_001318087.1:c.805G>T	NP_001305016.1:p.Ala269Ser
NM_001318088.1:c.-157G>T	NP_001305017.1:n.-157G>T
NM_001365135.1:c.805G>T	NP_001352064.1:p.Ala269Ser
NR_027400.2:n.990G>T
NR_134502.1:n.623+367G>T
XM_011520304.2:c.805G>T	XP_011518606.1:p.Ala269Ser
XR_001747940.2:n.930G>T
XR_002957158.1:n.930G>T
NM_000543.5:c.805G>T MANE Select	NP_000534.3:p.Ala269Ser
NM_001007593.3:c.802G>T	NP_001007594.2:p.Ala268Ser
NM_001318087.2:c.805G>T	NP_001305016.1:p.Ala269Ser
NM_001318088.2:c.-157G>T	NP_001305017.1:n.-157G>T
NM_001365135.2:c.805G>T	NP_001352064.1:p.Ala269Ser
NR_027400.3:n.930G>T
NR_134502.2:n.563+367G>T