Canonical Allele Identifier: CA472909773

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413201A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391971A>C , CM000673.2:g.6391971A>C	GRCh38
NC_000011.9:g.6413201A>C , CM000673.1:g.6413201A>C	GRCh37
NC_000011.8:g.6369777A>C	NCBI36
NG_011780.1:g.6547A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.906A>C MANE Select	ENSP00000340409.4:p.Thr302=
ENST00000342245.8:c.906A>C	ENSP00000340409.4:p.Thr302=
ENST00000526280.1:c.95A>C
ENST00000527275.5:c.903A>C	ENSP00000435350.1:p.Thr301=
ENST00000530395.1:c.87A>C	ENSP00000431479.1:p.Thr29=
ENST00000531303.5:c.438+468A>C	ENSP00000432625.1:n.438+468A>C
ENST00000533123.5:c.906A>C	ENSP00000435950.1:p.Thr302=
ENST00000533196.1:n.375-35A>C
ENST00000534405.5:c.906A>C	ENSP00000434353.1:p.Thr302=
NM_000543.4:c.906A>C	NP_000534.3:p.Thr302=
NM_001007593.2:c.903A>C	NP_001007594.2:p.Thr301=
XM_005253075.3:c.906A>C	XP_005253132.1:p.Thr302=
XM_011520303.1:c.906A>C	XP_011518605.1:p.Thr302=
XM_011520304.1:c.906A>C	XP_011518606.1:p.Thr302=
XR_930886.1:n.1204A>C
NM_001318087.1:c.906A>C	NP_001305016.1:p.Thr302=
NM_001318088.1:c.-56A>C	NP_001305017.1:n.-56A>C
NM_001365135.1:c.906A>C	NP_001352064.1:p.Thr302=
NR_027400.2:n.1091A>C
NR_134502.1:n.623+468A>C
XM_011520304.2:c.906A>C	XP_011518606.1:p.Thr302=
XR_001747940.2:n.1031A>C
XR_002957158.1:n.1031A>C
NM_000543.5:c.906A>C MANE Select	NP_000534.3:p.Thr302=
NM_001007593.3:c.903A>C	NP_001007594.2:p.Thr301=
NM_001318087.2:c.906A>C	NP_001305016.1:p.Thr302=
NM_001318088.2:c.-56A>C	NP_001305017.1:n.-56A>C
NM_001365135.2:c.906A>C	NP_001352064.1:p.Thr302=
NR_027400.3:n.1031A>C
NR_134502.2:n.563+468A>C