Canonical Allele Identifier: CA379374599

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6414920C>A (hg19) ; chr11:g.6393690C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393690C>A , CM000673.2:g.6393690C>A	GRCh38
NC_000011.9:g.6414920C>A , CM000673.1:g.6414920C>A	GRCh37
NC_000011.8:g.6371496C>A	NCBI36
NG_011780.1:g.8266C>A
NG_029615.1:g.30725G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1337C>A MANE Select	ENSP00000340409.4:p.Ala446Asp
ENST00000342245.8:c.1337C>A	ENSP00000340409.4:p.Ala446Asp
ENST00000526280.1:c.394C>A
ENST00000527275.5:c.1334C>A	ENSP00000435350.1:p.Ala445Asp
ENST00000531303.5:c.*168C>A	ENSP00000432625.1:n.*168C>A
ENST00000531336.1:n.169C>A
ENST00000532367.1:n.173C>A
ENST00000533123.5:c.*64C>A	ENSP00000435950.1:n.*64C>A
ENST00000534405.5:c.*168C>A	ENSP00000434353.1:n.*168C>A
NM_000543.4:c.1337C>A	NP_000534.3:p.Ala446Asp
NM_001007593.2:c.1334C>A	NP_001007594.2:p.Ala445Asp
XM_005253075.3:c.1337C>A	XP_005253132.1:p.Ala446Asp
XM_011520303.1:c.1205C>A	XP_011518605.1:p.Ala402Asp
XM_011520304.1:c.1205C>A	XP_011518606.1:p.Ala402Asp
XR_930886.1:n.1675C>A
NM_001318087.1:c.1337C>A	NP_001305016.1:p.Ala446Asp
NM_001318088.1:c.416C>A	NP_001305017.1:p.Ala139Asp
NM_001365135.1:c.1205C>A	NP_001352064.1:p.Ala402Asp
NR_027400.2:n.1350C>A
NR_134502.1:n.869C>A
XM_011520304.2:c.1205C>A	XP_011518606.1:p.Ala402Asp
XR_001747940.2:n.1502C>A
XR_002957158.1:n.1502C>A
NM_000543.5:c.1337C>A MANE Select	NP_000534.3:p.Ala446Asp
NM_001007593.3:c.1334C>A	NP_001007594.2:p.Ala445Asp
NM_001318087.2:c.1337C>A	NP_001305016.1:p.Ala446Asp
NM_001318088.2:c.416C>A	NP_001305017.1:p.Ala139Asp
NM_001365135.2:c.1205C>A	NP_001352064.1:p.Ala402Asp
NR_027400.3:n.1290C>A
NR_134502.2:n.809C>A