Canonical Allele Identifier: CA873270669

Gene: SSR4

Linked Data

• dbSNP Id: rs1213174946
• gnomAD v3: X-153797955-CTCCTT-C
• gnomAD v4: X-153797955-CTCCTT-C
• MyVariant Identifiers: chrX:g.153797956_153797960del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153797962_153797966del , CM000685.2:g.153797962_153797966del	GRCh38
NC_000023.10:g.153063417_153063421del , CM000685.1:g.153063417_153063421del	GRCh37
NC_000023.9:g.152716611_152716615del	NCBI36
NG_041795.1:g.8788_8792del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.352-109_352-105del MANE Select	ENSP00000359103.3:n.352-109_352-105del
ENST00000320857.7:c.352-109_352-105del	ENSP00000317331.3:n.352-109_352-105del
ENST00000370085.3:c.277-109_277-105del	ENSP00000359102.3:n.277-109_277-105del
ENST00000370086.7:c.352-109_352-105del	ENSP00000359103.3:n.352-109_352-105del
ENST00000370087.5:c.352-109_352-105del	ENSP00000359104.1:n.352-109_352-105del
ENST00000447375.1:n.192-109_192-105del
ENST00000460616.5:n.2060-109_2060-105del
ENST00000471880.5:n.555-109_555-105del
ENST00000482902.5:n.2179-109_2179-105del
ENST00000485612.5:n.467-109_467-105del
ENST00000486204.5:n.424-109_424-105del
NM_001204526.1:c.385-109_385-105del	NP_001191455.1:n.385-109_385-105del
NM_001204527.1:c.376-109_376-105del	NP_001191456.1:n.376-109_376-105del
NM_006280.2:c.352-109_352-105del	NP_006271.1:n.352-109_352-105del
NR_037927.1:n.697-109_697-105del
XM_011531186.1:c.352-109_352-105del	XP_011529488.1:n.352-109_352-105del
XM_011531187.1:c.352-109_352-105del	XP_011529489.1:n.352-109_352-105del
XM_017029756.1:c.163-109_163-105del	XP_016885245.1:n.163-109_163-105del
XM_017029757.1:c.163-109_163-105del	XP_016885246.1:n.163-109_163-105del
XM_024452428.1:c.163-109_163-105del	XP_024308196.1:n.163-109_163-105del
NM_001204527.2:c.376-109_376-105del	NP_001191456.1:n.376-109_376-105del
NM_006280.3:c.352-109_352-105del MANE Select	NP_006271.1:n.352-109_352-105del