Canonical Allele Identifier: CA379375570

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415265A>C (hg19) ; chr11:g.6394035A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394035A>C , CM000673.2:g.6394035A>C	GRCh38
NC_000011.9:g.6415265A>C , CM000673.1:g.6415265A>C	GRCh37
NC_000011.8:g.6371841A>C	NCBI36
NG_011780.1:g.8611A>C
NG_029615.1:g.30380T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1480A>C MANE Select	ENSP00000340409.4:p.Asn494His
ENST00000342245.8:c.1480A>C	ENSP00000340409.4:p.Asn494His
ENST00000526280.1:c.537A>C
ENST00000527275.5:c.1477A>C	ENSP00000435350.1:p.Asn493His
ENST00000531303.5:c.*311A>C	ENSP00000432625.1:n.*311A>C
ENST00000531336.1:n.312A>C
ENST00000532367.1:n.316A>C
ENST00000533123.5:c.*207A>C	ENSP00000435950.1:n.*207A>C
ENST00000534405.5:c.*311A>C	ENSP00000434353.1:n.*311A>C
NM_000543.4:c.1480A>C	NP_000534.3:p.Asn494His
NM_001007593.2:c.1477A>C	NP_001007594.2:p.Asn493His
XM_005253075.3:c.1480A>C	XP_005253132.1:p.Asn494His
XM_011520303.1:c.1348A>C	XP_011518605.1:p.Asn450His
XM_011520304.1:c.1348A>C	XP_011518606.1:p.Asn450His
NM_001318087.1:c.1480A>C	NP_001305016.1:p.Asn494His
NM_001318088.1:c.559A>C	NP_001305017.1:p.Asn187His
NM_001365135.1:c.1348A>C	NP_001352064.1:p.Asn450His
NR_027400.2:n.1493A>C
NR_134502.1:n.1012A>C
XM_011520304.2:c.1348A>C	XP_011518606.1:p.Asn450His
XR_001747940.2:n.1645A>C
XR_002957158.1:n.1847A>C
NM_000543.5:c.1480A>C MANE Select	NP_000534.3:p.Asn494His
NM_001007593.3:c.1477A>C	NP_001007594.2:p.Asn493His
NM_001318087.2:c.1480A>C	NP_001305016.1:p.Asn494His
NM_001318088.2:c.559A>C	NP_001305017.1:p.Asn187His
NM_001365135.2:c.1348A>C	NP_001352064.1:p.Asn450His
NR_027400.3:n.1433A>C
NR_134502.2:n.952A>C