Canonical Allele Identifier: CA379371272

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413212G>C (hg19) ; chr11:g.6391982G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391982G>C , CM000673.2:g.6391982G>C	GRCh38
NC_000011.9:g.6413212G>C , CM000673.1:g.6413212G>C	GRCh37
NC_000011.8:g.6369788G>C	NCBI36
NG_011780.1:g.6558G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.917G>C MANE Select	ENSP00000340409.4:p.Arg306Thr
ENST00000342245.8:c.917G>C	ENSP00000340409.4:p.Arg306Thr
ENST00000526280.1:c.106G>C
ENST00000527275.5:c.914G>C	ENSP00000435350.1:p.Arg305Thr
ENST00000530395.1:c.98G>C	ENSP00000431479.1:p.Arg33Thr
ENST00000531303.5:c.438+479G>C	ENSP00000432625.1:n.438+479G>C
ENST00000533123.5:c.917G>C	ENSP00000435950.1:p.Arg306Thr
ENST00000533196.1:n.375-24G>C
ENST00000534405.5:c.917G>C	ENSP00000434353.1:p.Arg306Thr
NM_000543.4:c.917G>C	NP_000534.3:p.Arg306Thr
NM_001007593.2:c.914G>C	NP_001007594.2:p.Arg305Thr
XM_005253075.3:c.917G>C	XP_005253132.1:p.Arg306Thr
XM_011520303.1:c.917G>C	XP_011518605.1:p.Arg306Thr
XM_011520304.1:c.917G>C	XP_011518606.1:p.Arg306Thr
XR_930886.1:n.1215G>C
NM_001318087.1:c.917G>C	NP_001305016.1:p.Arg306Thr
NM_001318088.1:c.-45G>C	NP_001305017.1:n.-45G>C
NM_001365135.1:c.917G>C	NP_001352064.1:p.Arg306Thr
NR_027400.2:n.1102G>C
NR_134502.1:n.623+479G>C
XM_011520304.2:c.917G>C	XP_011518606.1:p.Arg306Thr
XR_001747940.2:n.1042G>C
XR_002957158.1:n.1042G>C
NM_000543.5:c.917G>C MANE Select	NP_000534.3:p.Arg306Thr
NM_001007593.3:c.914G>C	NP_001007594.2:p.Arg305Thr
NM_001318087.2:c.917G>C	NP_001305016.1:p.Arg306Thr
NM_001318088.2:c.-45G>C	NP_001305017.1:n.-45G>C
NM_001365135.2:c.917G>C	NP_001352064.1:p.Arg306Thr
NR_027400.3:n.1042G>C
NR_134502.2:n.563+479G>C