Canonical Allele Identifier: CA2466480470
Gene: SSR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153797958C= , CM000685.2:g.153797958C= GRCh38
NC_000023.10:g.153063413C= , CM000685.1:g.153063413C= GRCh37
NC_000023.9:g.152716607C= NCBI36
NG_041795.1:g.8784C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370086.8:c.352-113C= MANE Select ENSP00000359103.3:n.352-113C=
ENST00000320857.7:c.352-113C= ENSP00000317331.3:n.352-113C=
ENST00000370085.3:c.277-113C= ENSP00000359102.3:n.277-113C=
ENST00000370086.7:c.352-113C= ENSP00000359103.3:n.352-113C=
ENST00000370087.5:c.352-113C= ENSP00000359104.1:n.352-113C=
ENST00000447375.1:n.192-113C=
ENST00000460616.5:n.2060-113C=
ENST00000471880.5:n.555-113C=
ENST00000482902.5:n.2179-113C=
ENST00000485612.5:n.467-113C=
ENST00000486204.5:n.424-113C=
NM_001204526.1:c.385-113C= NP_001191455.1:n.385-113C=
NM_001204527.1:c.376-113C= NP_001191456.1:n.376-113C=
NM_006280.2:c.352-113C= NP_006271.1:n.352-113C=
NR_037927.1:n.697-113C=
XM_011531186.1:c.352-113C= XP_011529488.1:n.352-113C=
XM_011531187.1:c.352-113C= XP_011529489.1:n.352-113C=
XM_017029756.1:c.163-113C= XP_016885245.1:n.163-113C=
XM_017029757.1:c.163-113C= XP_016885246.1:n.163-113C=
XM_024452428.1:c.163-113C= XP_024308196.1:n.163-113C=
NM_001204527.2:c.376-113C= NP_001191456.1:n.376-113C=
NM_006280.3:c.352-113C= MANE Select NP_006271.1:n.352-113C=