Canonical Allele Identifier: CA2612222621

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6393088-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393088T>C , CM000673.2:g.6393088T>C	GRCh38
NC_000011.9:g.6414318T>C , CM000673.1:g.6414318T>C	GRCh37
NC_000011.8:g.6370894T>C	NCBI36
NG_011780.1:g.7664T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1092-128T>C MANE Select	ENSP00000340409.4:n.1092-128T>C
ENST00000342245.8:c.1092-128T>C	ENSP00000340409.4:n.1092-128T>C
ENST00000526280.1:c.321-529T>C
ENST00000527275.5:c.1089-128T>C	ENSP00000435350.1:n.1089-128T>C
ENST00000531303.5:c.439-128T>C	ENSP00000432625.1:n.439-128T>C
ENST00000533123.5:c.1092-529T>C	ENSP00000435950.1:n.1092-529T>C
ENST00000534405.5:c.1132-128T>C	ENSP00000434353.1:n.1132-128T>C
NM_000543.4:c.1092-128T>C	NP_000534.3:n.1092-128T>C
NM_001007593.2:c.1089-128T>C	NP_001007594.2:n.1089-128T>C
XM_005253075.3:c.1092-128T>C	XP_005253132.1:n.1092-128T>C
XM_011520303.1:c.1132-529T>C	XP_011518605.1:n.1132-529T>C
XM_011520304.1:c.1132-529T>C	XP_011518606.1:n.1132-529T>C
XR_930886.1:n.1430-128T>C
NM_001318087.1:c.1092-128T>C	NP_001305016.1:n.1092-128T>C
NM_001318088.1:c.171-128T>C	NP_001305017.1:n.171-128T>C
NM_001365135.1:c.1132-529T>C	NP_001352064.1:n.1132-529T>C
NR_027400.2:n.1277-529T>C
NR_134502.1:n.624-128T>C
XM_011520304.2:c.1132-529T>C	XP_011518606.1:n.1132-529T>C
XR_001747940.2:n.1257-128T>C
XR_002957158.1:n.1257-128T>C
NM_000543.5:c.1092-128T>C MANE Select	NP_000534.3:n.1092-128T>C
NM_001007593.3:c.1089-128T>C	NP_001007594.2:n.1089-128T>C
NM_001318087.2:c.1092-128T>C	NP_001305016.1:n.1092-128T>C
NM_001318088.2:c.171-128T>C	NP_001305017.1:n.171-128T>C
NM_001365135.2:c.1132-529T>C	NP_001352064.1:n.1132-529T>C
NR_027400.3:n.1217-529T>C
NR_134502.2:n.564-128T>C