Canonical Allele Identifier: CA379376914

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415667T>A (hg19) ; chr11:g.6394437T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394437T>A , CM000673.2:g.6394437T>A	GRCh38
NC_000011.9:g.6415667T>A , CM000673.1:g.6415667T>A	GRCh37
NC_000011.8:g.6372243T>A	NCBI36
NG_011780.1:g.9013T>A
NG_029615.1:g.29978A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1726T>A MANE Select	ENSP00000340409.4:p.Tyr576Asn
ENST00000342245.8:c.1726T>A	ENSP00000340409.4:p.Tyr576Asn
ENST00000526280.1:c.783T>A
ENST00000527275.5:c.1723T>A	ENSP00000435350.1:p.Tyr575Asn
ENST00000531303.5:c.*577T>A	ENSP00000432625.1:n.*577T>A
ENST00000533123.5:c.*453T>A	ENSP00000435950.1:n.*453T>A
ENST00000534405.5:c.*557T>A	ENSP00000434353.1:n.*557T>A
NM_000543.4:c.1726T>A	NP_000534.3:p.Tyr576Asn
NM_001007593.2:c.1723T>A	NP_001007594.2:p.Tyr575Asn
XM_005253075.3:c.*219T>A	XP_005253132.1:n.*219T>A
XM_011520303.1:c.1594T>A	XP_011518605.1:p.Tyr532Asn
XM_011520304.1:c.*219T>A	XP_011518606.1:n.*219T>A
NM_001318087.1:c.*219T>A	NP_001305016.1:n.*219T>A
NM_001318088.1:c.805T>A	NP_001305017.1:p.Tyr269Asn
NM_001365135.1:c.1594T>A	NP_001352064.1:p.Tyr532Asn
NR_027400.2:n.1739T>A
NR_134502.1:n.1278T>A
XM_011520304.2:c.*219T>A	XP_011518606.1:n.*219T>A
XR_001747940.2:n.1911T>A
XR_002957158.1:n.2093T>A
NM_000543.5:c.1726T>A MANE Select	NP_000534.3:p.Tyr576Asn
NM_001007593.3:c.1723T>A	NP_001007594.2:p.Tyr575Asn
NM_001318087.2:c.*219T>A	NP_001305016.1:n.*219T>A
NM_001318088.2:c.805T>A	NP_001305017.1:p.Tyr269Asn
NM_001365135.2:c.1594T>A	NP_001352064.1:p.Tyr532Asn
NR_027400.3:n.1679T>A
NR_134502.2:n.1218T>A