Canonical Allele Identifier: CA379370363

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391685C>A , CM000673.2:g.6391685C>A	GRCh38
NC_000011.9:g.6412915C>A , CM000673.1:g.6412915C>A	GRCh37
NC_000011.8:g.6369491C>A	NCBI36
NG_011780.1:g.6261C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000543.5:c.620C>A MANE Select	NP_000534.3:p.Thr207Asn
ENST00000342245.9:c.620C>A MANE Select	ENSP00000340409.4:p.Thr207Asn
NM_000543.4:c.620C>A	NP_000534.3:p.Thr207Asn
NM_001007593.2:c.617C>A	NP_001007594.2:p.Thr206Asn
NM_001007593.3:c.617C>A	NP_001007594.2:p.Thr206Asn
NM_001318087.1:c.620C>A	NP_001305016.1:p.Thr207Asn
NM_001318087.2:c.620C>A	NP_001305016.1:p.Thr207Asn
NM_001318088.1:c.-342C>A	NP_001305017.1:n.-342C>A
NM_001318088.2:c.-342C>A	NP_001305017.1:n.-342C>A
NM_001365135.1:c.620C>A	NP_001352064.1:p.Thr207Asn
NM_001365135.2:c.620C>A	NP_001352064.1:p.Thr207Asn
NR_027400.2:n.805C>A
NR_027400.3:n.745C>A
NR_134502.1:n.623+182C>A
NR_134502.2:n.563+182C>A
ENST00000342245.8:c.620C>A	ENSP00000340409.4:p.Thr207Asn
ENST00000527275.5:c.617C>A	ENSP00000435350.1:p.Thr206Asn
ENST00000530395.1:c.-95-105C>A	ENSP00000431479.1:n.-95-105C>A
ENST00000531303.5:c.438+182C>A	ENSP00000432625.1:n.438+182C>A
ENST00000533123.5:c.620C>A	ENSP00000435950.1:p.Thr207Asn
ENST00000533196.1:n.375-321C>A
ENST00000534405.5:c.620C>A	ENSP00000434353.1:p.Thr207Asn
XM_005253075.3:c.620C>A	XP_005253132.1:p.Thr207Asn
XM_011520303.1:c.620C>A	XP_011518605.1:p.Thr207Asn
XM_011520304.1:c.620C>A	XP_011518606.1:p.Thr207Asn
XM_011520304.2:c.620C>A	XP_011518606.1:p.Thr207Asn
XR_001747940.2:n.745C>A
XR_002957158.1:n.745C>A
XR_930886.1:n.918C>A