Canonical Allele Identifier: CA472909811

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6412958T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391728T>G , CM000673.2:g.6391728T>G	GRCh38
NC_000011.9:g.6412958T>G , CM000673.1:g.6412958T>G	GRCh37
NC_000011.8:g.6369534T>G	NCBI36
NG_011780.1:g.6304T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.663T>G MANE Select	ENSP00000340409.4:p.Pro221=
ENST00000342245.8:c.663T>G	ENSP00000340409.4:p.Pro221=
ENST00000527275.5:c.660T>G	ENSP00000435350.1:p.Pro220=
ENST00000530395.1:c.-95-62T>G	ENSP00000431479.1:n.-95-62T>G
ENST00000531303.5:c.438+225T>G	ENSP00000432625.1:n.438+225T>G
ENST00000533123.5:c.663T>G	ENSP00000435950.1:p.Pro221=
ENST00000533196.1:n.375-278T>G
ENST00000534405.5:c.663T>G	ENSP00000434353.1:p.Pro221=
NM_000543.4:c.663T>G	NP_000534.3:p.Pro221=
NM_001007593.2:c.660T>G	NP_001007594.2:p.Pro220=
XM_005253075.3:c.663T>G	XP_005253132.1:p.Pro221=
XM_011520303.1:c.663T>G	XP_011518605.1:p.Pro221=
XM_011520304.1:c.663T>G	XP_011518606.1:p.Pro221=
XR_930886.1:n.961T>G
NM_001318087.1:c.663T>G	NP_001305016.1:p.Pro221=
NM_001318088.1:c.-299T>G	NP_001305017.1:n.-299T>G
NM_001365135.1:c.663T>G	NP_001352064.1:p.Pro221=
NR_027400.2:n.848T>G
NR_134502.1:n.623+225T>G
XM_011520304.2:c.663T>G	XP_011518606.1:p.Pro221=
XR_001747940.2:n.788T>G
XR_002957158.1:n.788T>G
NM_000543.5:c.663T>G MANE Select	NP_000534.3:p.Pro221=
NM_001007593.3:c.660T>G	NP_001007594.2:p.Pro220=
NM_001318087.2:c.663T>G	NP_001305016.1:p.Pro221=
NM_001318088.2:c.-299T>G	NP_001305017.1:n.-299T>G
NM_001365135.2:c.663T>G	NP_001352064.1:p.Pro221=
NR_027400.3:n.788T>G
NR_134502.2:n.563+225T>G