Canonical Allele Identifier: CA2612221020

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6390734-GCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390735_6390737del , CM000673.2:g.6390735_6390737del	GRCh38
NC_000011.9:g.6411965_6411967del , CM000673.1:g.6411965_6411967del	GRCh37
NC_000011.8:g.6368541_6368543del	NCBI36
NG_011780.1:g.5311_5313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.137_139del MANE Select	ENSP00000340409.4:p.Ala46_Leu47delinsVal
ENST00000342245.8:c.137_139del	ENSP00000340409.4:p.Ala46_Leu47delinsVal
ENST00000527275.5:c.137_139del	ENSP00000435350.1:p.Ala46_Leu47delinsVal
ENST00000530395.1:c.-96+96_-96+98del	ENSP00000431479.1:n.-96+96_-96+98del
ENST00000531303.5:c.137_139del	ENSP00000432625.1:p.Ala46_Leu47delinsVal
ENST00000533123.5:c.137_139del	ENSP00000435950.1:p.Ala46_Leu47delinsVal
ENST00000533196.1:n.296_298del
ENST00000534405.5:c.137_139del	ENSP00000434353.1:p.Ala46_Leu47delinsVal
NM_000543.4:c.137_139del	NP_000534.3:p.Ala46_Leu47delinsVal
NM_001007593.2:c.137_139del	NP_001007594.2:p.Ala46_Leu47delinsVal
XM_005253075.3:c.137_139del	XP_005253132.1:p.Ala46_Leu47delinsVal
XM_011520303.1:c.137_139del	XP_011518605.1:p.Ala46_Leu47delinsVal
XM_011520304.1:c.137_139del	XP_011518606.1:p.Ala46_Leu47delinsVal
XR_930886.1:n.435_437del
NM_001318087.1:c.137_139del	NP_001305016.1:p.Ala46_Leu47delinsVal
NM_001318088.1:c.-825_-823del	NP_001305017.1:n.-825_-823del
NM_001365135.1:c.137_139del	NP_001352064.1:p.Ala46_Leu47delinsVal
NR_027400.2:n.322_324del
NR_134502.1:n.322_324del
XM_011520304.2:c.137_139del	XP_011518606.1:p.Ala46_Leu47delinsVal
XR_001747940.2:n.262_264del
XR_002957158.1:n.262_264del
NM_000543.5:c.137_139del MANE Select	NP_000534.3:p.Ala46_Leu47delinsVal
NM_001007593.3:c.137_139del	NP_001007594.2:p.Ala46_Leu47delinsVal
NM_001318087.2:c.137_139del	NP_001305016.1:p.Ala46_Leu47delinsVal
NM_001318088.2:c.-825_-823del	NP_001305017.1:n.-825_-823del
NM_001365135.2:c.137_139del	NP_001352064.1:p.Ala46_Leu47delinsVal
NR_027400.3:n.262_264del
NR_134502.2:n.262_264del