Canonical Allele Identifier: CA472910012

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415249T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394019T>C , CM000673.2:g.6394019T>C	GRCh38
NC_000011.9:g.6415249T>C , CM000673.1:g.6415249T>C	GRCh37
NC_000011.8:g.6371825T>C	NCBI36
NG_011780.1:g.8595T>C
NG_029615.1:g.30396A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1464T>C MANE Select	ENSP00000340409.4:p.Thr488=
ENST00000342245.8:c.1464T>C	ENSP00000340409.4:p.Thr488=
ENST00000526280.1:c.521T>C
ENST00000527275.5:c.1461T>C	ENSP00000435350.1:p.Thr487=
ENST00000531303.5:c.*295T>C	ENSP00000432625.1:n.*295T>C
ENST00000531336.1:n.296T>C
ENST00000532367.1:n.300T>C
ENST00000533123.5:c.*191T>C	ENSP00000435950.1:n.*191T>C
ENST00000534405.5:c.*295T>C	ENSP00000434353.1:n.*295T>C
NM_000543.4:c.1464T>C	NP_000534.3:p.Thr488=
NM_001007593.2:c.1461T>C	NP_001007594.2:p.Thr487=
XM_005253075.3:c.1464T>C	XP_005253132.1:p.Thr488=
XM_011520303.1:c.1332T>C	XP_011518605.1:p.Thr444=
XM_011520304.1:c.1332T>C	XP_011518606.1:p.Thr444=
XR_930886.1:n.1802T>C
NM_001318087.1:c.1464T>C	NP_001305016.1:p.Thr488=
NM_001318088.1:c.543T>C	NP_001305017.1:p.Thr181=
NM_001365135.1:c.1332T>C	NP_001352064.1:p.Thr444=
NR_027400.2:n.1477T>C
NR_134502.1:n.996T>C
XM_011520304.2:c.1332T>C	XP_011518606.1:p.Thr444=
XR_001747940.2:n.1629T>C
XR_002957158.1:n.1831T>C
NM_000543.5:c.1464T>C MANE Select	NP_000534.3:p.Thr488=
NM_001007593.3:c.1461T>C	NP_001007594.2:p.Thr487=
NM_001318087.2:c.1464T>C	NP_001305016.1:p.Thr488=
NM_001318088.2:c.543T>C	NP_001305017.1:p.Thr181=
NM_001365135.2:c.1332T>C	NP_001352064.1:p.Thr444=
NR_027400.3:n.1417T>C
NR_134502.2:n.936T>C