Canonical Allele Identifier: CA379375877

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415452G>T (hg19) ; chr11:g.6394222G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394222G>T , CM000673.2:g.6394222G>T	GRCh38
NC_000011.9:g.6415452G>T , CM000673.1:g.6415452G>T	GRCh37
NC_000011.8:g.6372028G>T	NCBI36
NG_011780.1:g.8798G>T
NG_029615.1:g.30193C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1511G>T MANE Select	ENSP00000340409.4:p.Gly504Val
ENST00000342245.8:c.1511G>T	ENSP00000340409.4:p.Gly504Val
ENST00000526280.1:c.568G>T
ENST00000527275.5:c.1508G>T	ENSP00000435350.1:p.Gly503Val
ENST00000531303.5:c.*362G>T	ENSP00000432625.1:n.*362G>T
ENST00000531336.1:n.499G>T
ENST00000533123.5:c.*238G>T	ENSP00000435950.1:n.*238G>T
ENST00000534405.5:c.*342G>T	ENSP00000434353.1:n.*342G>T
NM_000543.4:c.1511G>T	NP_000534.3:p.Gly504Val
NM_001007593.2:c.1508G>T	NP_001007594.2:p.Gly503Val
XM_005253075.3:c.*4G>T	XP_005253132.1:n.*4G>T
XM_011520303.1:c.1379G>T	XP_011518605.1:p.Gly460Val
XM_011520304.1:c.*4G>T	XP_011518606.1:n.*4G>T
NM_001318087.1:c.*4G>T	NP_001305016.1:n.*4G>T
NM_001318088.1:c.590G>T	NP_001305017.1:p.Gly197Val
NM_001365135.1:c.1379G>T	NP_001352064.1:p.Gly460Val
NR_027400.2:n.1524G>T
NR_134502.1:n.1063G>T
XM_011520304.2:c.*4G>T	XP_011518606.1:n.*4G>T
XR_001747940.2:n.1696G>T
XR_002957158.1:n.1878G>T
NM_000543.5:c.1511G>T MANE Select	NP_000534.3:p.Gly504Val
NM_001007593.3:c.1508G>T	NP_001007594.2:p.Gly503Val
NM_001318087.2:c.*4G>T	NP_001305016.1:n.*4G>T
NM_001318088.2:c.590G>T	NP_001305017.1:p.Gly197Val
NM_001365135.2:c.1379G>T	NP_001352064.1:p.Gly460Val
NR_027400.3:n.1464G>T
NR_134502.2:n.1003G>T