Canonical Allele Identifier: CA10553198
Gene: SSR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153794653G>A , CM000685.2:g.153794653G>A GRCh38
NC_000023.10:g.153060108G>A , CM000685.1:g.153060108G>A GRCh37
NC_000023.9:g.152713302G>A NCBI36
NG_041795.1:g.5479G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001204526.1:c.20-21G>A NP_001191455.1:n.20-21G>A
NM_001204527.1:c.11-21G>A NP_001191456.1:n.11-21G>A
NM_001204527.2:c.11-21G>A NP_001191456.1:n.11-21G>A
NM_006280.2:c.-35G>A NP_006271.1:n.-35G>A
NR_037927.1:n.138-21G>A
ENST00000320857.7:c.-14-21G>A ENSP00000317331.3:n.-14-21G>A
ENST00000370086.7:c.-35G>A ENSP00000359103.3:n.-35G>A
ENST00000370087.5:c.-14-21G>A ENSP00000359104.1:n.-14-21G>A
ENST00000482902.5:n.138-21G>A
ENST00000491833.5:n.161-21G>A
XM_011531186.1:c.-14-21G>A XP_011529488.1:n.-14-21G>A
XM_011531187.1:c.-14-21G>A XP_011529489.1:n.-14-21G>A
XM_017029756.1:c.-974-21G>A XP_016885245.1:n.-974-21G>A
XM_024452428.1:c.-974-21G>A XP_024308196.1:n.-974-21G>A