Canonical Allele Identifier: CA379376464

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415542A>T (hg19) ; chr11:g.6394312A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394312A>T , CM000673.2:g.6394312A>T	GRCh38
NC_000011.9:g.6415542A>T , CM000673.1:g.6415542A>T	GRCh37
NC_000011.8:g.6372118A>T	NCBI36
NG_011780.1:g.8888A>T
NG_029615.1:g.30103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1601A>T MANE Select	ENSP00000340409.4:p.His534Leu
ENST00000342245.8:c.1601A>T	ENSP00000340409.4:p.His534Leu
ENST00000526280.1:c.658A>T
ENST00000527275.5:c.1598A>T	ENSP00000435350.1:p.His533Leu
ENST00000531303.5:c.*452A>T	ENSP00000432625.1:n.*452A>T
ENST00000531336.1:n.589A>T
ENST00000533123.5:c.*328A>T	ENSP00000435950.1:n.*328A>T
ENST00000534405.5:c.*432A>T	ENSP00000434353.1:n.*432A>T
NM_000543.4:c.1601A>T	NP_000534.3:p.His534Leu
NM_001007593.2:c.1598A>T	NP_001007594.2:p.His533Leu
XM_005253075.3:c.*94A>T	XP_005253132.1:n.*94A>T
XM_011520303.1:c.1469A>T	XP_011518605.1:p.His490Leu
XM_011520304.1:c.*94A>T	XP_011518606.1:n.*94A>T
NM_001318087.1:c.*94A>T	NP_001305016.1:n.*94A>T
NM_001318088.1:c.680A>T	NP_001305017.1:p.His227Leu
NM_001365135.1:c.1469A>T	NP_001352064.1:p.His490Leu
NR_027400.2:n.1614A>T
NR_134502.1:n.1153A>T
XM_011520304.2:c.*94A>T	XP_011518606.1:n.*94A>T
XR_001747940.2:n.1786A>T
XR_002957158.1:n.1968A>T
NM_000543.5:c.1601A>T MANE Select	NP_000534.3:p.His534Leu
NM_001007593.3:c.1598A>T	NP_001007594.2:p.His533Leu
NM_001318087.2:c.*94A>T	NP_001305016.1:n.*94A>T
NM_001318088.2:c.680A>T	NP_001305017.1:p.His227Leu
NM_001365135.2:c.1469A>T	NP_001352064.1:p.His490Leu
NR_027400.3:n.1554A>T
NR_134502.2:n.1093A>T