Canonical Allele Identifier: CA379375829

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415445A>T (hg19) ; chr11:g.6394215A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394215A>T , CM000673.2:g.6394215A>T	GRCh38
NC_000011.9:g.6415445A>T , CM000673.1:g.6415445A>T	GRCh37
NC_000011.8:g.6372021A>T	NCBI36
NG_011780.1:g.8791A>T
NG_029615.1:g.30200T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1504A>T MANE Select	ENSP00000340409.4:p.Ile502Leu
ENST00000342245.8:c.1504A>T	ENSP00000340409.4:p.Ile502Leu
ENST00000526280.1:c.561A>T
ENST00000527275.5:c.1501A>T	ENSP00000435350.1:p.Ile501Leu
ENST00000531303.5:c.*355A>T	ENSP00000432625.1:n.*355A>T
ENST00000531336.1:n.492A>T
ENST00000533123.5:c.*231A>T	ENSP00000435950.1:n.*231A>T
ENST00000534405.5:c.*335A>T	ENSP00000434353.1:n.*335A>T
NM_000543.4:c.1504A>T	NP_000534.3:p.Ile502Leu
NM_001007593.2:c.1501A>T	NP_001007594.2:p.Ile501Leu
XM_005253075.3:c.1524A>T	XP_005253132.1:p.Lys508Asn
XM_011520303.1:c.1372A>T	XP_011518605.1:p.Ile458Leu
XM_011520304.1:c.1392A>T	XP_011518606.1:p.Lys464Asn
NM_001318087.1:c.1524A>T	NP_001305016.1:p.Lys508Asn
NM_001318088.1:c.583A>T	NP_001305017.1:p.Ile195Leu
NM_001365135.1:c.1372A>T	NP_001352064.1:p.Ile458Leu
NR_027400.2:n.1517A>T
NR_134502.1:n.1056A>T
XM_011520304.2:c.1392A>T	XP_011518606.1:p.Lys464Asn
XR_001747940.2:n.1689A>T
XR_002957158.1:n.1871A>T
NM_000543.5:c.1504A>T MANE Select	NP_000534.3:p.Ile502Leu
NM_001007593.3:c.1501A>T	NP_001007594.2:p.Ile501Leu
NM_001318087.2:c.1524A>T	NP_001305016.1:p.Lys508Asn
NM_001318088.2:c.583A>T	NP_001305017.1:p.Ile195Leu
NM_001365135.2:c.1372A>T	NP_001352064.1:p.Ile458Leu
NR_027400.3:n.1457A>T
NR_134502.2:n.996A>T