Canonical Allele Identifier: CA379366761

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390659C>T , CM000673.2:g.6390659C>T	GRCh38
NC_000011.9:g.6411889C>T , CM000673.1:g.6411889C>T	GRCh37
NC_000011.8:g.6368465C>T	NCBI36
NG_011780.1:g.5235C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000543.5:c.61C>T MANE Select	NP_000534.3:p.Gln21Ter
ENST00000342245.9:c.61C>T MANE Select	ENSP00000340409.4:p.Gln21Ter
NM_000543.4:c.61C>T	NP_000534.3:p.Gln21Ter
NM_001007593.2:c.61C>T	NP_001007594.2:p.Gln21Ter
NM_001007593.3:c.61C>T	NP_001007594.2:p.Gln21Ter
NM_001318087.1:c.61C>T	NP_001305016.1:p.Gln21Ter
NM_001318087.2:c.61C>T	NP_001305016.1:p.Gln21Ter
NM_001318088.1:c.-901C>T	NP_001305017.1:n.-901C>T
NM_001318088.2:c.-901C>T	NP_001305017.1:n.-901C>T
NM_001365135.1:c.61C>T	NP_001352064.1:p.Gln21Ter
NM_001365135.2:c.61C>T	NP_001352064.1:p.Gln21Ter
NR_027400.2:n.246C>T
NR_027400.3:n.186C>T
NR_134502.1:n.246C>T
NR_134502.2:n.186C>T
ENST00000342245.8:c.61C>T	ENSP00000340409.4:p.Gln21Ter
ENST00000527275.5:c.61C>T	ENSP00000435350.1:p.Gln21Ter
ENST00000530395.1:c.-96+20C>T	ENSP00000431479.1:n.-96+20C>T
ENST00000531303.5:c.61C>T	ENSP00000432625.1:p.Gln21Ter
ENST00000533123.5:c.61C>T	ENSP00000435950.1:p.Gln21Ter
ENST00000533196.1:n.220C>T
ENST00000534405.5:c.61C>T	ENSP00000434353.1:p.Gln21Ter
XM_005253075.3:c.61C>T	XP_005253132.1:p.Gln21Ter
XM_011520303.1:c.61C>T	XP_011518605.1:p.Gln21Ter
XM_011520304.1:c.61C>T	XP_011518606.1:p.Gln21Ter
XM_011520304.2:c.61C>T	XP_011518606.1:p.Gln21Ter
XR_001747940.2:n.186C>T
XR_002957158.1:n.186C>T
XR_930886.1:n.359C>T