Canonical Allele Identifier: CA597438105

Gene: SMPD1

Linked Data

• dbSNP Id: rs1330181005
• gnomAD v2: 11-6411781-C-T
• gnomAD v4: 11-6390551-C-T
• MyVariant Identifiers: chr11:g.6411781C>T (hg19) ; chr11:g.6390551C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390551C>T , CM000673.2:g.6390551C>T	GRCh38
NC_000011.9:g.6411781C>T , CM000673.1:g.6411781C>T	GRCh37
NC_000011.8:g.6368357C>T	NCBI36
NG_011780.1:g.5127C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.-48C>T MANE Select	ENSP00000340409.4:n.-48C>T
ENST00000342245.8:c.-48C>T	ENSP00000340409.4:n.-48C>T
ENST00000527275.5:c.-48C>T	ENSP00000435350.1:n.-48C>T
ENST00000530395.1:c.-184C>T	ENSP00000431479.1:n.-184C>T
ENST00000533123.5:c.-48C>T	ENSP00000435950.1:n.-48C>T
ENST00000533196.1:n.112C>T
ENST00000534405.5:c.-48C>T	ENSP00000434353.1:n.-48C>T
NM_000543.4:c.-48C>T	NP_000534.3:n.-48C>T
NM_001007593.2:c.-48C>T	NP_001007594.2:n.-48C>T
XM_005253075.3:c.-48C>T	XP_005253132.1:n.-48C>T
XM_011520303.1:c.-48C>T	XP_011518605.1:n.-48C>T
XM_011520304.1:c.-48C>T	XP_011518606.1:n.-48C>T
XR_930886.1:n.251C>T
NM_001318087.1:c.-48C>T	NP_001305016.1:n.-48C>T
NM_001318088.1:c.-1009C>T	NP_001305017.1:n.-1009C>T
NM_001365135.1:c.-48C>T	NP_001352064.1:n.-48C>T
NR_027400.2:n.138C>T
NR_134502.1:n.138C>T
XM_011520304.2:c.-48C>T	XP_011518606.1:n.-48C>T
XR_001747940.2:n.78C>T
XR_002957158.1:n.78C>T
NM_000543.5:c.-48C>T MANE Select	NP_000534.3:n.-48C>T
NM_001007593.3:c.-48C>T	NP_001007594.2:n.-48C>T
NM_001318087.2:c.-48C>T	NP_001305016.1:n.-48C>T
NM_001318088.2:c.-1009C>T	NP_001305017.1:n.-1009C>T
NM_001365135.2:c.-48C>T	NP_001352064.1:n.-48C>T
NR_027400.3:n.78C>T
NR_134502.2:n.78C>T