Canonical Allele Identifier: CA2503079368

Gene: SSR4

Linked Data

• gnomAD v4: X-153797949-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153797952del , CM000685.2:g.153797952del	GRCh38
NC_000023.10:g.153063407del , CM000685.1:g.153063407del	GRCh37
NC_000023.9:g.152716601del	NCBI36
NG_041795.1:g.8778del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370086.8:c.352-119del MANE Select	ENSP00000359103.3:n.352-119del
ENST00000320857.7:c.352-119del	ENSP00000317331.3:n.352-119del
ENST00000370085.3:c.277-119del	ENSP00000359102.3:n.277-119del
ENST00000370086.7:c.352-119del	ENSP00000359103.3:n.352-119del
ENST00000370087.5:c.352-119del	ENSP00000359104.1:n.352-119del
ENST00000447375.1:n.192-119del
ENST00000460616.5:n.2060-119del
ENST00000471880.5:n.555-119del
ENST00000482902.5:n.2179-119del
ENST00000485612.5:n.467-119del
ENST00000486204.5:n.424-119del
NM_001204526.1:c.385-119del	NP_001191455.1:n.385-119del
NM_001204527.1:c.376-119del	NP_001191456.1:n.376-119del
NM_006280.2:c.352-119del	NP_006271.1:n.352-119del
NR_037927.1:n.697-119del
XM_011531186.1:c.352-119del	XP_011529488.1:n.352-119del
XM_011531187.1:c.352-119del	XP_011529489.1:n.352-119del
XM_017029756.1:c.163-119del	XP_016885245.1:n.163-119del
XM_017029757.1:c.163-119del	XP_016885246.1:n.163-119del
XM_024452428.1:c.163-119del	XP_024308196.1:n.163-119del
NM_001204527.2:c.376-119del	NP_001191456.1:n.376-119del
NM_006280.3:c.352-119del MANE Select	NP_006271.1:n.352-119del