Canonical Allele Identifier: CA934779449

Gene: SMPD1

Linked Data

• dbSNP Id: rs775568984
• gnomAD v3: 11-6390705-T-TGGCGCTGGCGCTGGCGCTGGCGCTGGC
• gnomAD v4: 11-6390705-T-TGGCGCTGGCGCTGGCGCTGGCGCTGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390706_6390707insGCGCTGGCGCTGGCGCTGGCGCTGGCG , CM000673.2:g.6390706_6390707insGCGCTGGCGCTGGCGCTGGCGCTGGCG	GRCh38
NC_000011.9:g.6411936_6411937insGCGCTGGCGCTGGCGCTGGCGCTGGCG , CM000673.1:g.6411936_6411937insGCGCTGGCGCTGGCGCTGGCGCTGGCG	GRCh37
NC_000011.8:g.6368512_6368513insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NCBI36
NG_011780.1:g.5282_5283insGCGCTGGCGCTGGCGCTGGCGCTGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG MANE Select	ENSP00000340409.4:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla...
ENST00000342245.8:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	ENSP00000340409.4:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla...
ENST00000527275.5:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	ENSP00000435350.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla...
ENST00000530395.1:c.-96+67_-96+68insGCGCTGGCGCTGGCGCTGGCGCTGGCG	ENSP00000431479.1:n.-96+67_-96+68insGCGCTGGCGCTGGCGCTGGCGCTGG...
ENST00000531303.5:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	ENSP00000432625.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla...
ENST00000533123.5:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	ENSP00000435950.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla...
ENST00000533196.1:n.267_268insGCGCTGGCGCTGGCGCTGGCGCTGGCG
ENST00000534405.5:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	ENSP00000434353.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla...
NM_000543.4:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_000534.3:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NM_001007593.2:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001007594.2:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
XM_005253075.3:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	XP_005253132.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
XM_011520303.1:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	XP_011518605.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
XM_011520304.1:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	XP_011518606.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
XR_930886.1:n.406_407insGCGCTGGCGCTGGCGCTGGCGCTGGCG
NM_001318087.1:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001305016.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NM_001318088.1:c.-854_-853insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001305017.1:n.-854_-853insGCGCTGGCGCTGGCGCTGGCGCTGGCG
NM_001365135.1:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001352064.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NR_027400.2:n.293_294insGCGCTGGCGCTGGCGCTGGCGCTGGCG
NR_134502.1:n.293_294insGCGCTGGCGCTGGCGCTGGCGCTGGCG
XM_011520304.2:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	XP_011518606.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
XR_001747940.2:n.233_234insGCGCTGGCGCTGGCGCTGGCGCTGGCG
XR_002957158.1:n.233_234insGCGCTGGCGCTGGCGCTGGCGCTGGCG
NM_000543.5:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG MANE Select	NP_000534.3:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NM_001007593.3:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001007594.2:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NM_001318087.2:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001305016.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NM_001318088.2:c.-854_-853insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001305017.1:n.-854_-853insGCGCTGGCGCTGGCGCTGGCGCTGGCG
NM_001365135.2:c.108_109insGCGCTGGCGCTGGCGCTGGCGCTGGCG	NP_001352064.1:p.Val36_Leu37insAlaLeuAlaLeuAlaLeuAlaLeuAla
NR_027400.3:n.233_234insGCGCTGGCGCTGGCGCTGGCGCTGGCG
NR_134502.2:n.233_234insGCGCTGGCGCTGGCGCTGGCGCTGGCG