Canonical Allele Identifier: CA2612220908

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6390497-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390497T>C , CM000673.2:g.6390497T>C	GRCh38
NC_000011.9:g.6411727T>C , CM000673.1:g.6411727T>C	GRCh37
NC_000011.8:g.6368303T>C	NCBI36
NG_011780.1:g.5073T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.-102T>C MANE Select	ENSP00000340409.4:n.-102T>C
ENST00000342245.8:c.-102T>C	ENSP00000340409.4:n.-102T>C
ENST00000527275.5:c.-102T>C	ENSP00000435350.1:n.-102T>C
ENST00000530395.1:c.-238T>C	ENSP00000431479.1:n.-238T>C
ENST00000533196.1:n.58T>C
ENST00000534405.5:c.-102T>C	ENSP00000434353.1:n.-102T>C
NM_000543.4:c.-102T>C	NP_000534.3:n.-102T>C
NM_001007593.2:c.-102T>C	NP_001007594.2:n.-102T>C
XM_005253075.3:c.-102T>C	XP_005253132.1:n.-102T>C
XM_011520303.1:c.-102T>C	XP_011518605.1:n.-102T>C
XM_011520304.1:c.-102T>C	XP_011518606.1:n.-102T>C
XR_930886.1:n.197T>C
NM_001318087.1:c.-102T>C	NP_001305016.1:n.-102T>C
NM_001318088.1:c.-1063T>C	NP_001305017.1:n.-1063T>C
NM_001365135.1:c.-102T>C	NP_001352064.1:n.-102T>C
NR_027400.2:n.84T>C
NR_134502.1:n.84T>C
XM_011520304.2:c.-102T>C	XP_011518606.1:n.-102T>C
XR_001747940.2:n.24T>C
XR_002957158.1:n.24T>C
NM_000543.5:c.-102T>C MANE Select	NP_000534.3:n.-102T>C
NM_001007593.3:c.-102T>C	NP_001007594.2:n.-102T>C
NM_001318087.2:c.-102T>C	NP_001305016.1:n.-102T>C
NM_001318088.2:c.-1063T>C	NP_001305017.1:n.-1063T>C
NM_001365135.2:c.-102T>C	NP_001352064.1:n.-102T>C
NR_027400.3:n.24T>C
NR_134502.2:n.24T>C