Canonical Allele Identifier: CA379376266

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415506A>C (hg19) ; chr11:g.6394276A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394276A>C , CM000673.2:g.6394276A>C	GRCh38
NC_000011.9:g.6415506A>C , CM000673.1:g.6415506A>C	GRCh37
NC_000011.8:g.6372082A>C	NCBI36
NG_011780.1:g.8852A>C
NG_029615.1:g.30139T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1565A>C MANE Select	ENSP00000340409.4:p.Asn522Thr
ENST00000342245.8:c.1565A>C	ENSP00000340409.4:p.Asn522Thr
ENST00000526280.1:c.622A>C
ENST00000527275.5:c.1562A>C	ENSP00000435350.1:p.Asn521Thr
ENST00000531303.5:c.*416A>C	ENSP00000432625.1:n.*416A>C
ENST00000531336.1:n.553A>C
ENST00000533123.5:c.*292A>C	ENSP00000435950.1:n.*292A>C
ENST00000534405.5:c.*396A>C	ENSP00000434353.1:n.*396A>C
NM_000543.4:c.1565A>C	NP_000534.3:p.Asn522Thr
NM_001007593.2:c.1562A>C	NP_001007594.2:p.Asn521Thr
XM_005253075.3:c.*58A>C	XP_005253132.1:n.*58A>C
XM_011520303.1:c.1433A>C	XP_011518605.1:p.Asn478Thr
XM_011520304.1:c.*58A>C	XP_011518606.1:n.*58A>C
NM_001318087.1:c.*58A>C	NP_001305016.1:n.*58A>C
NM_001318088.1:c.644A>C	NP_001305017.1:p.Asn215Thr
NM_001365135.1:c.1433A>C	NP_001352064.1:p.Asn478Thr
NR_027400.2:n.1578A>C
NR_134502.1:n.1117A>C
XM_011520304.2:c.*58A>C	XP_011518606.1:n.*58A>C
XR_001747940.2:n.1750A>C
XR_002957158.1:n.1932A>C
NM_000543.5:c.1565A>C MANE Select	NP_000534.3:p.Asn522Thr
NM_001007593.3:c.1562A>C	NP_001007594.2:p.Asn521Thr
NM_001318087.2:c.*58A>C	NP_001305016.1:n.*58A>C
NM_001318088.2:c.644A>C	NP_001305017.1:p.Asn215Thr
NM_001365135.2:c.1433A>C	NP_001352064.1:p.Asn478Thr
NR_027400.3:n.1518A>C
NR_134502.2:n.1057A>C