Canonical Allele Identifier: CA379371270

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413211A>T (hg19) ; chr11:g.6391981A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391981A>T , CM000673.2:g.6391981A>T	GRCh38
NC_000011.9:g.6413211A>T , CM000673.1:g.6413211A>T	GRCh37
NC_000011.8:g.6369787A>T	NCBI36
NG_011780.1:g.6557A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.916A>T MANE Select	ENSP00000340409.4:p.Arg306Trp
ENST00000342245.8:c.916A>T	ENSP00000340409.4:p.Arg306Trp
ENST00000526280.1:c.105A>T
ENST00000527275.5:c.913A>T	ENSP00000435350.1:p.Arg305Trp
ENST00000530395.1:c.97A>T	ENSP00000431479.1:p.Arg33Trp
ENST00000531303.5:c.438+478A>T	ENSP00000432625.1:n.438+478A>T
ENST00000533123.5:c.916A>T	ENSP00000435950.1:p.Arg306Trp
ENST00000533196.1:n.375-25A>T
ENST00000534405.5:c.916A>T	ENSP00000434353.1:p.Arg306Trp
NM_000543.4:c.916A>T	NP_000534.3:p.Arg306Trp
NM_001007593.2:c.913A>T	NP_001007594.2:p.Arg305Trp
XM_005253075.3:c.916A>T	XP_005253132.1:p.Arg306Trp
XM_011520303.1:c.916A>T	XP_011518605.1:p.Arg306Trp
XM_011520304.1:c.916A>T	XP_011518606.1:p.Arg306Trp
XR_930886.1:n.1214A>T
NM_001318087.1:c.916A>T	NP_001305016.1:p.Arg306Trp
NM_001318088.1:c.-46A>T	NP_001305017.1:n.-46A>T
NM_001365135.1:c.916A>T	NP_001352064.1:p.Arg306Trp
NR_027400.2:n.1101A>T
NR_134502.1:n.623+478A>T
XM_011520304.2:c.916A>T	XP_011518606.1:p.Arg306Trp
XR_001747940.2:n.1041A>T
XR_002957158.1:n.1041A>T
NM_000543.5:c.916A>T MANE Select	NP_000534.3:p.Arg306Trp
NM_001007593.3:c.913A>T	NP_001007594.2:p.Arg305Trp
NM_001318087.2:c.916A>T	NP_001305016.1:p.Arg306Trp
NM_001318088.2:c.-46A>T	NP_001305017.1:n.-46A>T
NM_001365135.2:c.916A>T	NP_001352064.1:p.Arg306Trp
NR_027400.3:n.1041A>T
NR_134502.2:n.563+478A>T