Canonical Allele Identifier: CA472736605

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413360G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392130G>C , CM000673.2:g.6392130G>C	GRCh38
NC_000011.9:g.6413360G>C , CM000673.1:g.6413360G>C	GRCh37
NC_000011.8:g.6369936G>C	NCBI36
NG_011780.1:g.6706G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1065G>C MANE Select	ENSP00000340409.4:p.Leu355=
ENST00000342245.8:c.1065G>C	ENSP00000340409.4:p.Leu355=
ENST00000526280.1:c.254G>C
ENST00000527275.5:c.1062G>C	ENSP00000435350.1:p.Leu354=
ENST00000531303.5:c.438+627G>C	ENSP00000432625.1:n.438+627G>C
ENST00000533123.5:c.1065G>C	ENSP00000435950.1:p.Leu355=
ENST00000534405.5:c.1065G>C	ENSP00000434353.1:p.Leu355=
NM_000543.4:c.1065G>C	NP_000534.3:p.Leu355=
NM_001007593.2:c.1062G>C	NP_001007594.2:p.Leu354=
XM_005253075.3:c.1065G>C	XP_005253132.1:p.Leu355=
XM_011520303.1:c.1065G>C	XP_011518605.1:p.Leu355=
XM_011520304.1:c.1065G>C	XP_011518606.1:p.Leu355=
XR_930886.1:n.1363G>C
NM_001318087.1:c.1065G>C	NP_001305016.1:p.Leu355=
NM_001318088.1:c.104G>C	NP_001305017.1:p.Cys35Ser
NM_001365135.1:c.1065G>C	NP_001352064.1:p.Leu355=
NR_027400.2:n.1250G>C
NR_134502.1:n.623+627G>C
XM_011520304.2:c.1065G>C	XP_011518606.1:p.Leu355=
XR_001747940.2:n.1190G>C
XR_002957158.1:n.1190G>C
NM_000543.5:c.1065G>C MANE Select	NP_000534.3:p.Leu355=
NM_001007593.3:c.1062G>C	NP_001007594.2:p.Leu354=
NM_001318087.2:c.1065G>C	NP_001305016.1:p.Leu355=
NM_001318088.2:c.104G>C	NP_001305017.1:p.Cys35Ser
NM_001365135.2:c.1065G>C	NP_001352064.1:p.Leu355=
NR_027400.3:n.1190G>C
NR_134502.2:n.563+627G>C