Canonical Allele Identifier: CA379371249

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413199A>T (hg19) ; chr11:g.6391969A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391969A>T , CM000673.2:g.6391969A>T	GRCh38
NC_000011.9:g.6413199A>T , CM000673.1:g.6413199A>T	GRCh37
NC_000011.8:g.6369775A>T	NCBI36
NG_011780.1:g.6545A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.904A>T MANE Select	ENSP00000340409.4:p.Thr302Ser
ENST00000342245.8:c.904A>T	ENSP00000340409.4:p.Thr302Ser
ENST00000526280.1:c.93A>T
ENST00000527275.5:c.901A>T	ENSP00000435350.1:p.Thr301Ser
ENST00000530395.1:c.85A>T	ENSP00000431479.1:p.Thr29Ser
ENST00000531303.5:c.438+466A>T	ENSP00000432625.1:n.438+466A>T
ENST00000533123.5:c.904A>T	ENSP00000435950.1:p.Thr302Ser
ENST00000533196.1:n.375-37A>T
ENST00000534405.5:c.904A>T	ENSP00000434353.1:p.Thr302Ser
NM_000543.4:c.904A>T	NP_000534.3:p.Thr302Ser
NM_001007593.2:c.901A>T	NP_001007594.2:p.Thr301Ser
XM_005253075.3:c.904A>T	XP_005253132.1:p.Thr302Ser
XM_011520303.1:c.904A>T	XP_011518605.1:p.Thr302Ser
XM_011520304.1:c.904A>T	XP_011518606.1:p.Thr302Ser
XR_930886.1:n.1202A>T
NM_001318087.1:c.904A>T	NP_001305016.1:p.Thr302Ser
NM_001318088.1:c.-58A>T	NP_001305017.1:n.-58A>T
NM_001365135.1:c.904A>T	NP_001352064.1:p.Thr302Ser
NR_027400.2:n.1089A>T
NR_134502.1:n.623+466A>T
XM_011520304.2:c.904A>T	XP_011518606.1:p.Thr302Ser
XR_001747940.2:n.1029A>T
XR_002957158.1:n.1029A>T
NM_000543.5:c.904A>T MANE Select	NP_000534.3:p.Thr302Ser
NM_001007593.3:c.901A>T	NP_001007594.2:p.Thr301Ser
NM_001318087.2:c.904A>T	NP_001305016.1:p.Thr302Ser
NM_001318088.2:c.-58A>T	NP_001305017.1:n.-58A>T
NM_001365135.2:c.904A>T	NP_001352064.1:p.Thr302Ser
NR_027400.3:n.1029A>T
NR_134502.2:n.563+466A>T