Canonical Allele Identifier: CA2612224410

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394881-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394881C>T , CM000673.2:g.6394881C>T	GRCh38
NC_000011.9:g.6416111C>T , CM000673.1:g.6416111C>T	GRCh37
NC_000011.8:g.6372687C>T	NCBI36
NG_011780.1:g.9457C>T
NG_029615.1:g.29534G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*274C>T MANE Select	ENSP00000340409.4:n.*274C>T
ENST00000342245.8:c.*274C>T	ENSP00000340409.4:n.*274C>T
ENST00000526280.1:c.1227C>T
ENST00000533123.5:c.*897C>T	ENSP00000435950.1:n.*897C>T
ENST00000534405.5:c.*1001C>T	ENSP00000434353.1:n.*1001C>T
NM_000543.4:c.*274C>T	NP_000534.3:n.*274C>T
NM_001007593.2:c.*274C>T	NP_001007594.2:n.*274C>T
XM_011520303.1:c.*274C>T	XP_011518605.1:n.*274C>T
NM_001318087.1:c.*663C>T	NP_001305016.1:n.*663C>T
NM_001318088.1:c.*274C>T	NP_001305017.1:n.*274C>T
NM_001365135.1:c.*274C>T	NP_001352064.1:n.*274C>T
NR_027400.2:n.2183C>T
NR_134502.1:n.1722C>T
XR_001747940.2:n.2355C>T
XR_002957158.1:n.2537C>T
NM_000543.5:c.*274C>T MANE Select	NP_000534.3:n.*274C>T
NM_001007593.3:c.*274C>T	NP_001007594.2:n.*274C>T
NM_001318087.2:c.*663C>T	NP_001305016.1:n.*663C>T
NM_001318088.2:c.*274C>T	NP_001305017.1:n.*274C>T
NM_001365135.2:c.*274C>T	NP_001352064.1:n.*274C>T
NR_027400.3:n.2123C>T
NR_134502.2:n.1662C>T