Canonical Allele Identifier: CA379376075

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415476T>C (hg19) ; chr11:g.6394246T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394246T>C , CM000673.2:g.6394246T>C	GRCh38
NC_000011.9:g.6415476T>C , CM000673.1:g.6415476T>C	GRCh37
NC_000011.8:g.6372052T>C	NCBI36
NG_011780.1:g.8822T>C
NG_029615.1:g.30169A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1535T>C MANE Select	ENSP00000340409.4:p.Val512Ala
ENST00000342245.8:c.1535T>C	ENSP00000340409.4:p.Val512Ala
ENST00000526280.1:c.592T>C
ENST00000527275.5:c.1532T>C	ENSP00000435350.1:p.Val511Ala
ENST00000531303.5:c.*386T>C	ENSP00000432625.1:n.*386T>C
ENST00000531336.1:n.523T>C
ENST00000533123.5:c.*262T>C	ENSP00000435950.1:n.*262T>C
ENST00000534405.5:c.*366T>C	ENSP00000434353.1:n.*366T>C
NM_000543.4:c.1535T>C	NP_000534.3:p.Val512Ala
NM_001007593.2:c.1532T>C	NP_001007594.2:p.Val511Ala
XM_005253075.3:c.*28T>C	XP_005253132.1:n.*28T>C
XM_011520303.1:c.1403T>C	XP_011518605.1:p.Val468Ala
XM_011520304.1:c.*28T>C	XP_011518606.1:n.*28T>C
NM_001318087.1:c.*28T>C	NP_001305016.1:n.*28T>C
NM_001318088.1:c.614T>C	NP_001305017.1:p.Val205Ala
NM_001365135.1:c.1403T>C	NP_001352064.1:p.Val468Ala
NR_027400.2:n.1548T>C
NR_134502.1:n.1087T>C
XM_011520304.2:c.*28T>C	XP_011518606.1:n.*28T>C
XR_001747940.2:n.1720T>C
XR_002957158.1:n.1902T>C
NM_000543.5:c.1535T>C MANE Select	NP_000534.3:p.Val512Ala
NM_001007593.3:c.1532T>C	NP_001007594.2:p.Val511Ala
NM_001318087.2:c.*28T>C	NP_001305016.1:n.*28T>C
NM_001318088.2:c.614T>C	NP_001305017.1:p.Val205Ala
NM_001365135.2:c.1403T>C	NP_001352064.1:p.Val468Ala
NR_027400.3:n.1488T>C
NR_134502.2:n.1027T>C