Canonical Allele Identifier: CA472909839

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413246T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392016T>A , CM000673.2:g.6392016T>A	GRCh38
NC_000011.9:g.6413246T>A , CM000673.1:g.6413246T>A	GRCh37
NC_000011.8:g.6369822T>A	NCBI36
NG_011780.1:g.6592T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.951T>A MANE Select	ENSP00000340409.4:p.Ala317=
ENST00000342245.8:c.951T>A	ENSP00000340409.4:p.Ala317=
ENST00000526280.1:c.140T>A
ENST00000527275.5:c.948T>A	ENSP00000435350.1:p.Ala316=
ENST00000530395.1:c.132T>A	ENSP00000431479.1:p.Ala44=
ENST00000531303.5:c.438+513T>A	ENSP00000432625.1:n.438+513T>A
ENST00000533123.5:c.951T>A	ENSP00000435950.1:p.Ala317=
ENST00000533196.1:n.385T>A
ENST00000534405.5:c.951T>A	ENSP00000434353.1:p.Ala317=
NM_000543.4:c.951T>A	NP_000534.3:p.Ala317=
NM_001007593.2:c.948T>A	NP_001007594.2:p.Ala316=
XM_005253075.3:c.951T>A	XP_005253132.1:p.Ala317=
XM_011520303.1:c.951T>A	XP_011518605.1:p.Ala317=
XM_011520304.1:c.951T>A	XP_011518606.1:p.Ala317=
XR_930886.1:n.1249T>A
NM_001318087.1:c.951T>A	NP_001305016.1:p.Ala317=
NM_001318088.1:c.-11T>A	NP_001305017.1:n.-11T>A
NM_001365135.1:c.951T>A	NP_001352064.1:p.Ala317=
NR_027400.2:n.1136T>A
NR_134502.1:n.623+513T>A
XM_011520304.2:c.951T>A	XP_011518606.1:p.Ala317=
XR_001747940.2:n.1076T>A
XR_002957158.1:n.1076T>A
NM_000543.5:c.951T>A MANE Select	NP_000534.3:p.Ala317=
NM_001007593.3:c.948T>A	NP_001007594.2:p.Ala316=
NM_001318087.2:c.951T>A	NP_001305016.1:p.Ala317=
NM_001318088.2:c.-11T>A	NP_001305017.1:n.-11T>A
NM_001365135.2:c.951T>A	NP_001352064.1:p.Ala317=
NR_027400.3:n.1076T>A
NR_134502.2:n.563+513T>A