Canonical Allele Identifier: CA379374412

Gene: SMPD1

Linked Data

• COSMIC: COSM3687482 ; COSM3687483
• MyVariant Identifiers: chr11:g.6414890G>T (hg19) ; chr11:g.6393660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393660G>T , CM000673.2:g.6393660G>T	GRCh38
NC_000011.9:g.6414890G>T , CM000673.1:g.6414890G>T	GRCh37
NC_000011.8:g.6371466G>T	NCBI36
NG_011780.1:g.8236G>T
NG_029615.1:g.30755C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1307G>T MANE Select	ENSP00000340409.4:p.Ser436Ile
ENST00000342245.8:c.1307G>T	ENSP00000340409.4:p.Ser436Ile
ENST00000526280.1:c.364G>T
ENST00000527275.5:c.1304G>T	ENSP00000435350.1:p.Ser435Ile
ENST00000531303.5:c.*138G>T	ENSP00000432625.1:n.*138G>T
ENST00000531336.1:n.139G>T
ENST00000532367.1:n.143G>T
ENST00000533123.5:c.*34G>T	ENSP00000435950.1:n.*34G>T
ENST00000534405.5:c.*138G>T	ENSP00000434353.1:n.*138G>T
NM_000543.4:c.1307G>T	NP_000534.3:p.Ser436Ile
NM_001007593.2:c.1304G>T	NP_001007594.2:p.Ser435Ile
XM_005253075.3:c.1307G>T	XP_005253132.1:p.Ser436Ile
XM_011520303.1:c.1175G>T	XP_011518605.1:p.Ser392Ile
XM_011520304.1:c.1175G>T	XP_011518606.1:p.Ser392Ile
XR_930886.1:n.1645G>T
NM_001318087.1:c.1307G>T	NP_001305016.1:p.Ser436Ile
NM_001318088.1:c.386G>T	NP_001305017.1:p.Ser129Ile
NM_001365135.1:c.1175G>T	NP_001352064.1:p.Ser392Ile
NR_027400.2:n.1320G>T
NR_134502.1:n.839G>T
XM_011520304.2:c.1175G>T	XP_011518606.1:p.Ser392Ile
XR_001747940.2:n.1472G>T
XR_002957158.1:n.1472G>T
NM_000543.5:c.1307G>T MANE Select	NP_000534.3:p.Ser436Ile
NM_001007593.3:c.1304G>T	NP_001007594.2:p.Ser435Ile
NM_001318087.2:c.1307G>T	NP_001305016.1:p.Ser436Ile
NM_001318088.2:c.386G>T	NP_001305017.1:p.Ser129Ile
NM_001365135.2:c.1175G>T	NP_001352064.1:p.Ser392Ile
NR_027400.3:n.1260G>T
NR_134502.2:n.779G>T