Canonical Allele Identifier: CA415187037
Gene: SSR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798110C>G , CM000685.2:g.153798110C>G GRCh38
NC_000023.10:g.153063565C>G , CM000685.1:g.153063565C>G GRCh37
NC_000023.9:g.152716759C>G NCBI36
NG_041795.1:g.8936C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370086.8:c.391C>G MANE Select ENSP00000359103.3:p.Leu131Val
ENST00000320857.7:c.391C>G ENSP00000317331.3:p.Leu131Val
ENST00000370085.3:c.316C>G ENSP00000359102.3:p.Leu106Val
ENST00000370086.7:c.391C>G ENSP00000359103.3:p.Leu131Val
ENST00000370087.5:c.391C>G ENSP00000359104.1:p.Leu131Val
ENST00000447375.1:n.231C>G
ENST00000460616.5:n.2099C>G
ENST00000471880.5:n.594C>G
ENST00000482902.5:n.2218C>G
ENST00000485612.5:n.506C>G
ENST00000486204.5:n.463C>G
NM_001204526.1:c.424C>G NP_001191455.1:p.Leu142Val
NM_001204527.1:c.415C>G NP_001191456.1:p.Leu139Val
NM_006280.2:c.391C>G NP_006271.1:p.Leu131Val
NR_037927.1:n.736C>G
XM_011531186.1:c.391C>G XP_011529488.1:p.Leu131Val
XM_011531187.1:c.391C>G XP_011529489.1:p.Leu131Val
XM_017029756.1:c.202C>G XP_016885245.1:p.Leu68Val
XM_017029757.1:c.202C>G XP_016885246.1:p.Leu68Val
XM_024452428.1:c.202C>G XP_024308196.1:p.Leu68Val
NM_001204527.2:c.415C>G NP_001191456.1:p.Leu139Val
NM_006280.3:c.391C>G MANE Select NP_006271.1:p.Leu131Val