Canonical Allele Identifier: CA2612224186

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394687-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394687G>T , CM000673.2:g.6394687G>T	GRCh38
NC_000011.9:g.6415917G>T , CM000673.1:g.6415917G>T	GRCh37
NC_000011.8:g.6372493G>T	NCBI36
NG_011780.1:g.9263G>T
NG_029615.1:g.29728C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*80G>T MANE Select	ENSP00000340409.4:n.*80G>T
ENST00000342245.8:c.*80G>T	ENSP00000340409.4:n.*80G>T
ENST00000526280.1:c.1033G>T
ENST00000527275.5:c.*80G>T	ENSP00000435350.1:n.*80G>T
ENST00000531303.5:c.*827G>T	ENSP00000432625.1:n.*827G>T
ENST00000533123.5:c.*703G>T	ENSP00000435950.1:n.*703G>T
ENST00000534405.5:c.*807G>T	ENSP00000434353.1:n.*807G>T
NM_000543.4:c.*80G>T	NP_000534.3:n.*80G>T
NM_001007593.2:c.*80G>T	NP_001007594.2:n.*80G>T
XM_011520303.1:c.*80G>T	XP_011518605.1:n.*80G>T
NM_001318087.1:c.*469G>T	NP_001305016.1:n.*469G>T
NM_001318088.1:c.*80G>T	NP_001305017.1:n.*80G>T
NM_001365135.1:c.*80G>T	NP_001352064.1:n.*80G>T
NR_027400.2:n.1989G>T
NR_134502.1:n.1528G>T
XR_001747940.2:n.2161G>T
XR_002957158.1:n.2343G>T
NM_000543.5:c.*80G>T MANE Select	NP_000534.3:n.*80G>T
NM_001007593.3:c.*80G>T	NP_001007594.2:n.*80G>T
NM_001318087.2:c.*469G>T	NP_001305016.1:n.*469G>T
NM_001318088.2:c.*80G>T	NP_001305017.1:n.*80G>T
NM_001365135.2:c.*80G>T	NP_001352064.1:n.*80G>T
NR_027400.3:n.1929G>T
NR_134502.2:n.1468G>T