Canonical Allele Identifier: CA379371564

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413292T>A (hg19) ; chr11:g.6392062T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392062T>A , CM000673.2:g.6392062T>A	GRCh38
NC_000011.9:g.6413292T>A , CM000673.1:g.6413292T>A	GRCh37
NC_000011.8:g.6369868T>A	NCBI36
NG_011780.1:g.6638T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.997T>A MANE Select	ENSP00000340409.4:p.Phe333Ile
ENST00000342245.8:c.997T>A	ENSP00000340409.4:p.Phe333Ile
ENST00000526280.1:c.186T>A
ENST00000527275.5:c.994T>A	ENSP00000435350.1:p.Phe332Ile
ENST00000531303.5:c.438+559T>A	ENSP00000432625.1:n.438+559T>A
ENST00000533123.5:c.997T>A	ENSP00000435950.1:p.Phe333Ile
ENST00000534405.5:c.997T>A	ENSP00000434353.1:p.Phe333Ile
NM_000543.4:c.997T>A	NP_000534.3:p.Phe333Ile
NM_001007593.2:c.994T>A	NP_001007594.2:p.Phe332Ile
XM_005253075.3:c.997T>A	XP_005253132.1:p.Phe333Ile
XM_011520303.1:c.997T>A	XP_011518605.1:p.Phe333Ile
XM_011520304.1:c.997T>A	XP_011518606.1:p.Phe333Ile
XR_930886.1:n.1295T>A
NM_001318087.1:c.997T>A	NP_001305016.1:p.Phe333Ile
NM_001318088.1:c.36T>A	NP_001305017.1:p.Pro12=
NM_001365135.1:c.997T>A	NP_001352064.1:p.Phe333Ile
NR_027400.2:n.1182T>A
NR_134502.1:n.623+559T>A
XM_011520304.2:c.997T>A	XP_011518606.1:p.Phe333Ile
XR_001747940.2:n.1122T>A
XR_002957158.1:n.1122T>A
NM_000543.5:c.997T>A MANE Select	NP_000534.3:p.Phe333Ile
NM_001007593.3:c.994T>A	NP_001007594.2:p.Phe332Ile
NM_001318087.2:c.997T>A	NP_001305016.1:p.Phe333Ile
NM_001318088.2:c.36T>A	NP_001305017.1:p.Pro12=
NM_001365135.2:c.997T>A	NP_001352064.1:p.Phe333Ile
NR_027400.3:n.1122T>A
NR_134502.2:n.563+559T>A