Canonical Allele Identifier: CA472909407
Gene: SMPD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.6412775C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391545C>G , CM000673.2:g.6391545C>G GRCh38
NC_000011.9:g.6412775C>G , CM000673.1:g.6412775C>G GRCh37
NC_000011.8:g.6369351C>G NCBI36
NG_011780.1:g.6121C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.480C>G MANE Select ENSP00000340409.4:p.Gly160=
ENST00000342245.8:c.480C>G ENSP00000340409.4:p.Gly160=
ENST00000527275.5:c.477C>G ENSP00000435350.1:p.Gly159=
ENST00000530395.1:c.-95-245C>G ENSP00000431479.1:n.-95-245C>G
ENST00000531303.5:c.438+42C>G ENSP00000432625.1:n.438+42C>G
ENST00000533123.5:c.480C>G ENSP00000435950.1:p.Gly160=
ENST00000533196.1:n.375-461C>G
ENST00000534405.5:c.480C>G ENSP00000434353.1:p.Gly160=
NM_000543.4:c.480C>G NP_000534.3:p.Gly160=
NM_001007593.2:c.477C>G NP_001007594.2:p.Gly159=
XM_005253075.3:c.480C>G XP_005253132.1:p.Gly160=
XM_011520303.1:c.480C>G XP_011518605.1:p.Gly160=
XM_011520304.1:c.480C>G XP_011518606.1:p.Gly160=
XR_930886.1:n.778C>G
NM_001318087.1:c.480C>G NP_001305016.1:p.Gly160=
NM_001318088.1:c.-482C>G NP_001305017.1:n.-482C>G
NM_001365135.1:c.480C>G NP_001352064.1:p.Gly160=
NR_027400.2:n.665C>G
NR_134502.1:n.623+42C>G
XM_011520304.2:c.480C>G XP_011518606.1:p.Gly160=
XR_001747940.2:n.605C>G
XR_002957158.1:n.605C>G
NM_000543.5:c.480C>G MANE Select NP_000534.3:p.Gly160=
NM_001007593.3:c.477C>G NP_001007594.2:p.Gly159=
NM_001318087.2:c.480C>G NP_001305016.1:p.Gly160=
NM_001318088.2:c.-482C>G NP_001305017.1:n.-482C>G
NM_001365135.2:c.480C>G NP_001352064.1:p.Gly160=
NR_027400.3:n.605C>G
NR_134502.2:n.563+42C>G