Canonical Allele Identifier: CA472736615

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413372C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392142C>T , CM000673.2:g.6392142C>T	GRCh38
NC_000011.9:g.6413372C>T , CM000673.1:g.6413372C>T	GRCh37
NC_000011.8:g.6369948C>T	NCBI36
NG_011780.1:g.6718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1077C>T MANE Select	ENSP00000340409.4:p.Ala359=
ENST00000342245.8:c.1077C>T	ENSP00000340409.4:p.Ala359=
ENST00000526280.1:c.266C>T
ENST00000527275.5:c.1074C>T	ENSP00000435350.1:p.Ala358=
ENST00000531303.5:c.438+639C>T	ENSP00000432625.1:n.438+639C>T
ENST00000533123.5:c.1077C>T	ENSP00000435950.1:p.Ala359=
ENST00000534405.5:c.1077C>T	ENSP00000434353.1:p.Ala359=
NM_000543.4:c.1077C>T	NP_000534.3:p.Ala359=
NM_001007593.2:c.1074C>T	NP_001007594.2:p.Ala358=
XM_005253075.3:c.1077C>T	XP_005253132.1:p.Ala359=
XM_011520303.1:c.1077C>T	XP_011518605.1:p.Ala359=
XM_011520304.1:c.1077C>T	XP_011518606.1:p.Ala359=
XR_930886.1:n.1375C>T
NM_001318087.1:c.1077C>T	NP_001305016.1:p.Ala359=
NM_001318088.1:c.116C>T	NP_001305017.1:p.Pro39Leu
NM_001365135.1:c.1077C>T	NP_001352064.1:p.Ala359=
NR_027400.2:n.1262C>T
NR_134502.1:n.623+639C>T
XM_011520304.2:c.1077C>T	XP_011518606.1:p.Ala359=
XR_001747940.2:n.1202C>T
XR_002957158.1:n.1202C>T
NM_000543.5:c.1077C>T MANE Select	NP_000534.3:p.Ala359=
NM_001007593.3:c.1074C>T	NP_001007594.2:p.Ala358=
NM_001318087.2:c.1077C>T	NP_001305016.1:p.Ala359=
NM_001318088.2:c.116C>T	NP_001305017.1:p.Pro39Leu
NM_001365135.2:c.1077C>T	NP_001352064.1:p.Ala359=
NR_027400.3:n.1202C>T
NR_134502.2:n.563+639C>T