Canonical Allele Identifier: CA379376149

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415489T>A (hg19) ; chr11:g.6394259T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394259T>A , CM000673.2:g.6394259T>A	GRCh38
NC_000011.9:g.6415489T>A , CM000673.1:g.6415489T>A	GRCh37
NC_000011.8:g.6372065T>A	NCBI36
NG_011780.1:g.8835T>A
NG_029615.1:g.30156A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1548T>A MANE Select	ENSP00000340409.4:p.His516Gln
ENST00000342245.8:c.1548T>A	ENSP00000340409.4:p.His516Gln
ENST00000526280.1:c.605T>A
ENST00000527275.5:c.1545T>A	ENSP00000435350.1:p.His515Gln
ENST00000531303.5:c.*399T>A	ENSP00000432625.1:n.*399T>A
ENST00000531336.1:n.536T>A
ENST00000533123.5:c.*275T>A	ENSP00000435950.1:n.*275T>A
ENST00000534405.5:c.*379T>A	ENSP00000434353.1:n.*379T>A
NM_000543.4:c.1548T>A	NP_000534.3:p.His516Gln
NM_001007593.2:c.1545T>A	NP_001007594.2:p.His515Gln
XM_005253075.3:c.*41T>A	XP_005253132.1:n.*41T>A
XM_011520303.1:c.1416T>A	XP_011518605.1:p.His472Gln
XM_011520304.1:c.*41T>A	XP_011518606.1:n.*41T>A
NM_001318087.1:c.*41T>A	NP_001305016.1:n.*41T>A
NM_001318088.1:c.627T>A	NP_001305017.1:p.His209Gln
NM_001365135.1:c.1416T>A	NP_001352064.1:p.His472Gln
NR_027400.2:n.1561T>A
NR_134502.1:n.1100T>A
XM_011520304.2:c.*41T>A	XP_011518606.1:n.*41T>A
XR_001747940.2:n.1733T>A
XR_002957158.1:n.1915T>A
NM_000543.5:c.1548T>A MANE Select	NP_000534.3:p.His516Gln
NM_001007593.3:c.1545T>A	NP_001007594.2:p.His515Gln
NM_001318087.2:c.*41T>A	NP_001305016.1:n.*41T>A
NM_001318088.2:c.627T>A	NP_001305017.1:p.His209Gln
NM_001365135.2:c.1416T>A	NP_001352064.1:p.His472Gln
NR_027400.3:n.1501T>A
NR_134502.2:n.1040T>A