Canonical Allele Identifier: CA379374513

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6414905A>G (hg19) ; chr11:g.6393675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393675A>G , CM000673.2:g.6393675A>G	GRCh38
NC_000011.9:g.6414905A>G , CM000673.1:g.6414905A>G	GRCh37
NC_000011.8:g.6371481A>G	NCBI36
NG_011780.1:g.8251A>G
NG_029615.1:g.30740T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1322A>G MANE Select	ENSP00000340409.4:p.Tyr441Cys
ENST00000342245.8:c.1322A>G	ENSP00000340409.4:p.Tyr441Cys
ENST00000526280.1:c.379A>G
ENST00000527275.5:c.1319A>G	ENSP00000435350.1:p.Tyr440Cys
ENST00000531303.5:c.*153A>G	ENSP00000432625.1:n.*153A>G
ENST00000531336.1:n.154A>G
ENST00000532367.1:n.158A>G
ENST00000533123.5:c.*49A>G	ENSP00000435950.1:n.*49A>G
ENST00000534405.5:c.*153A>G	ENSP00000434353.1:n.*153A>G
NM_000543.4:c.1322A>G	NP_000534.3:p.Tyr441Cys
NM_001007593.2:c.1319A>G	NP_001007594.2:p.Tyr440Cys
XM_005253075.3:c.1322A>G	XP_005253132.1:p.Tyr441Cys
XM_011520303.1:c.1190A>G	XP_011518605.1:p.Tyr397Cys
XM_011520304.1:c.1190A>G	XP_011518606.1:p.Tyr397Cys
XR_930886.1:n.1660A>G
NM_001318087.1:c.1322A>G	NP_001305016.1:p.Tyr441Cys
NM_001318088.1:c.401A>G	NP_001305017.1:p.Tyr134Cys
NM_001365135.1:c.1190A>G	NP_001352064.1:p.Tyr397Cys
NR_027400.2:n.1335A>G
NR_134502.1:n.854A>G
XM_011520304.2:c.1190A>G	XP_011518606.1:p.Tyr397Cys
XR_001747940.2:n.1487A>G
XR_002957158.1:n.1487A>G
NM_000543.5:c.1322A>G MANE Select	NP_000534.3:p.Tyr441Cys
NM_001007593.3:c.1319A>G	NP_001007594.2:p.Tyr440Cys
NM_001318087.2:c.1322A>G	NP_001305016.1:p.Tyr441Cys
NM_001318088.2:c.401A>G	NP_001305017.1:p.Tyr134Cys
NM_001365135.2:c.1190A>G	NP_001352064.1:p.Tyr397Cys
NR_027400.3:n.1275A>G
NR_134502.2:n.794A>G