Canonical Allele Identifier: CA379371034

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413094G>C (hg19) ; chr11:g.6391864G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391864G>C , CM000673.2:g.6391864G>C	GRCh38
NC_000011.9:g.6413094G>C , CM000673.1:g.6413094G>C	GRCh37
NC_000011.8:g.6369670G>C	NCBI36
NG_011780.1:g.6440G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.799G>C MANE Select	ENSP00000340409.4:p.Gly267Arg
ENST00000342245.8:c.799G>C	ENSP00000340409.4:p.Gly267Arg
ENST00000527275.5:c.796G>C	ENSP00000435350.1:p.Gly266Arg
ENST00000530395.1:c.-21G>C	ENSP00000431479.1:n.-21G>C
ENST00000531303.5:c.438+361G>C	ENSP00000432625.1:n.438+361G>C
ENST00000533123.5:c.799G>C	ENSP00000435950.1:p.Gly267Arg
ENST00000533196.1:n.375-142G>C
ENST00000534405.5:c.799G>C	ENSP00000434353.1:p.Gly267Arg
NM_000543.4:c.799G>C	NP_000534.3:p.Gly267Arg
NM_001007593.2:c.796G>C	NP_001007594.2:p.Gly266Arg
XM_005253075.3:c.799G>C	XP_005253132.1:p.Gly267Arg
XM_011520303.1:c.799G>C	XP_011518605.1:p.Gly267Arg
XM_011520304.1:c.799G>C	XP_011518606.1:p.Gly267Arg
XR_930886.1:n.1097G>C
NM_001318087.1:c.799G>C	NP_001305016.1:p.Gly267Arg
NM_001318088.1:c.-163G>C	NP_001305017.1:n.-163G>C
NM_001365135.1:c.799G>C	NP_001352064.1:p.Gly267Arg
NR_027400.2:n.984G>C
NR_134502.1:n.623+361G>C
XM_011520304.2:c.799G>C	XP_011518606.1:p.Gly267Arg
XR_001747940.2:n.924G>C
XR_002957158.1:n.924G>C
NM_000543.5:c.799G>C MANE Select	NP_000534.3:p.Gly267Arg
NM_001007593.3:c.796G>C	NP_001007594.2:p.Gly266Arg
NM_001318087.2:c.799G>C	NP_001305016.1:p.Gly267Arg
NM_001318088.2:c.-163G>C	NP_001305017.1:n.-163G>C
NM_001365135.2:c.799G>C	NP_001352064.1:p.Gly267Arg
NR_027400.3:n.924G>C
NR_134502.2:n.563+361G>C