Canonical Allele Identifier: CA6949246
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 311764
dbSNP Id: rs143274967

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.36304412C>T , CM000675.2:g.36304412C>T GRCh38
NC_000013.10:g.36878549C>T , CM000675.1:g.36878549C>T GRCh37
NC_000013.9:g.35776549C>T NCBI36
NG_011559.1:g.70769G>A
NG_011559.2:g.70769G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000438666.7:c.1954G>A MANE Select ENSP00000406061.2:p.Asp652Asn
ENST00000650221.1:c.1954G>A ENSP00000497209.1:p.Asp652Asn
ENST00000355182.8:c.1954G>A ENSP00000347314.4:p.Asp652Asn
ENST00000438666.6:c.1954G>A ENSP00000406061.2:p.Asp652Asn
ENST00000451493.5:c.1954G>A ENSP00000414147.1:p.Asp652Asn
ENST00000491805.5:n.578G>A
ENST00000494062.2:c.1954G>A ENSP00000473599.1:p.Asp652Asn
NM_001142294.1:c.1954G>A NP_001135766.1:p.Asp652Asn
NM_001142295.1:c.1954G>A NP_001135767.1:p.Asp652Asn
NM_001142296.1:c.1954G>A NP_001135768.1:p.Asp652Asn
NM_015087.4:c.1954G>A NP_055902.1:p.Asp652Asn
XM_005266313.3:c.1954G>A XP_005266370.1:p.Asp652Asn
XM_005266314.2:c.1954G>A XP_005266371.1:p.Asp652Asn
XM_005266315.2:c.1954G>A XP_005266372.1:p.Asp652Asn
XM_005266316.2:c.1954G>A XP_005266373.1:p.Asp652Asn
XM_005266317.2:c.1954G>A XP_005266374.1:p.Asp652Asn
XM_011535012.1:c.1954G>A XP_011533314.1:p.Asp652Asn
XM_005266313.5:c.1954G>A XP_005266370.1:p.Asp652Asn
XM_005266314.3:c.1954G>A XP_005266371.1:p.Asp652Asn
XM_005266315.3:c.1954G>A XP_005266372.1:p.Asp652Asn
XM_005266317.3:c.1954G>A XP_005266374.1:p.Asp652Asn
XM_011535012.2:c.1954G>A XP_011533314.1:p.Asp652Asn
XM_024449334.1:c.1954G>A XP_024305102.1:p.Asp652Asn
XR_001749523.2:n.2297G>A
NM_015087.5:c.1954G>A MANE Select NP_055902.1:p.Asp652Asn
NM_001142296.2:c.1954G>A NP_001135768.1:p.Asp652Asn
NM_001142294.2:c.1954G>A NP_001135766.1:p.Asp652Asn
NM_001142295.2:c.1954G>A NP_001135767.1:p.Asp652Asn