Canonical Allele Identifier: CA379376963

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415679C>G (hg19) ; chr11:g.6394449C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394449C>G , CM000673.2:g.6394449C>G	GRCh38
NC_000011.9:g.6415679C>G , CM000673.1:g.6415679C>G	GRCh37
NC_000011.8:g.6372255C>G	NCBI36
NG_011780.1:g.9025C>G
NG_029615.1:g.29966G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1738C>G MANE Select	ENSP00000340409.4:p.His580Asp
ENST00000342245.8:c.1738C>G	ENSP00000340409.4:p.His580Asp
ENST00000526280.1:c.795C>G
ENST00000527275.5:c.1735C>G	ENSP00000435350.1:p.His579Asp
ENST00000531303.5:c.*589C>G	ENSP00000432625.1:n.*589C>G
ENST00000533123.5:c.*465C>G	ENSP00000435950.1:n.*465C>G
ENST00000534405.5:c.*569C>G	ENSP00000434353.1:n.*569C>G
NM_000543.4:c.1738C>G	NP_000534.3:p.His580Asp
NM_001007593.2:c.1735C>G	NP_001007594.2:p.His579Asp
XM_005253075.3:c.*231C>G	XP_005253132.1:n.*231C>G
XM_011520303.1:c.1606C>G	XP_011518605.1:p.His536Asp
XM_011520304.1:c.*231C>G	XP_011518606.1:n.*231C>G
NM_001318087.1:c.*231C>G	NP_001305016.1:n.*231C>G
NM_001318088.1:c.817C>G	NP_001305017.1:p.His273Asp
NM_001365135.1:c.1606C>G	NP_001352064.1:p.His536Asp
NR_027400.2:n.1751C>G
NR_134502.1:n.1290C>G
XM_011520304.2:c.*231C>G	XP_011518606.1:n.*231C>G
XR_001747940.2:n.1923C>G
XR_002957158.1:n.2105C>G
NM_000543.5:c.1738C>G MANE Select	NP_000534.3:p.His580Asp
NM_001007593.3:c.1735C>G	NP_001007594.2:p.His579Asp
NM_001318087.2:c.*231C>G	NP_001305016.1:n.*231C>G
NM_001318088.2:c.817C>G	NP_001305017.1:p.His273Asp
NM_001365135.2:c.1606C>G	NP_001352064.1:p.His536Asp
NR_027400.3:n.1691C>G
NR_134502.2:n.1230C>G