Canonical Allele Identifier: CA379374575

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6414916G>C (hg19) ; chr11:g.6393686G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393686G>C , CM000673.2:g.6393686G>C	GRCh38
NC_000011.9:g.6414916G>C , CM000673.1:g.6414916G>C	GRCh37
NC_000011.8:g.6371492G>C	NCBI36
NG_011780.1:g.8262G>C
NG_029615.1:g.30729C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1333G>C MANE Select	ENSP00000340409.4:p.Val445Leu
ENST00000342245.8:c.1333G>C	ENSP00000340409.4:p.Val445Leu
ENST00000526280.1:c.390G>C
ENST00000527275.5:c.1330G>C	ENSP00000435350.1:p.Val444Leu
ENST00000531303.5:c.*164G>C	ENSP00000432625.1:n.*164G>C
ENST00000531336.1:n.165G>C
ENST00000532367.1:n.169G>C
ENST00000533123.5:c.*60G>C	ENSP00000435950.1:n.*60G>C
ENST00000534405.5:c.*164G>C	ENSP00000434353.1:n.*164G>C
NM_000543.4:c.1333G>C	NP_000534.3:p.Val445Leu
NM_001007593.2:c.1330G>C	NP_001007594.2:p.Val444Leu
XM_005253075.3:c.1333G>C	XP_005253132.1:p.Val445Leu
XM_011520303.1:c.1201G>C	XP_011518605.1:p.Val401Leu
XM_011520304.1:c.1201G>C	XP_011518606.1:p.Val401Leu
XR_930886.1:n.1671G>C
NM_001318087.1:c.1333G>C	NP_001305016.1:p.Val445Leu
NM_001318088.1:c.412G>C	NP_001305017.1:p.Val138Leu
NM_001365135.1:c.1201G>C	NP_001352064.1:p.Val401Leu
NR_027400.2:n.1346G>C
NR_134502.1:n.865G>C
XM_011520304.2:c.1201G>C	XP_011518606.1:p.Val401Leu
XR_001747940.2:n.1498G>C
XR_002957158.1:n.1498G>C
NM_000543.5:c.1333G>C MANE Select	NP_000534.3:p.Val445Leu
NM_001007593.3:c.1330G>C	NP_001007594.2:p.Val444Leu
NM_001318087.2:c.1333G>C	NP_001305016.1:p.Val445Leu
NM_001318088.2:c.412G>C	NP_001305017.1:p.Val138Leu
NM_001365135.2:c.1201G>C	NP_001352064.1:p.Val401Leu
NR_027400.3:n.1286G>C
NR_134502.2:n.805G>C