Canonical Allele Identifier: CA2695065584

Gene: SSR4

Linked Data

• gnomAD v4: X-153798010-T-TCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798012_153798014dup , CM000685.2:g.153798012_153798014dup	GRCh38
NC_000023.10:g.153063467_153063469dup , CM000685.1:g.153063467_153063469dup	GRCh37
NC_000023.9:g.152716661_152716663dup	NCBI36
NG_041795.1:g.8838_8840dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.352-59_352-57dup MANE Select	ENSP00000359103.3:n.352-59_352-57dup
ENST00000320857.7:c.352-59_352-57dup	ENSP00000317331.3:n.352-59_352-57dup
ENST00000370085.3:c.277-59_277-57dup	ENSP00000359102.3:n.277-59_277-57dup
ENST00000370086.7:c.352-59_352-57dup	ENSP00000359103.3:n.352-59_352-57dup
ENST00000370087.5:c.352-59_352-57dup	ENSP00000359104.1:n.352-59_352-57dup
ENST00000447375.1:n.192-59_192-57dup
ENST00000460616.5:n.2060-59_2060-57dup
ENST00000471880.5:n.555-59_555-57dup
ENST00000482902.5:n.2179-59_2179-57dup
ENST00000485612.5:n.467-59_467-57dup
ENST00000486204.5:n.424-59_424-57dup
NM_001204526.1:c.385-59_385-57dup	NP_001191455.1:n.385-59_385-57dup
NM_001204527.1:c.376-59_376-57dup	NP_001191456.1:n.376-59_376-57dup
NM_006280.2:c.352-59_352-57dup	NP_006271.1:n.352-59_352-57dup
NR_037927.1:n.697-59_697-57dup
XM_011531186.1:c.352-59_352-57dup	XP_011529488.1:n.352-59_352-57dup
XM_011531187.1:c.352-59_352-57dup	XP_011529489.1:n.352-59_352-57dup
XM_017029756.1:c.163-59_163-57dup	XP_016885245.1:n.163-59_163-57dup
XM_017029757.1:c.163-59_163-57dup	XP_016885246.1:n.163-59_163-57dup
XM_024452428.1:c.163-59_163-57dup	XP_024308196.1:n.163-59_163-57dup
NM_001204527.2:c.376-59_376-57dup	NP_001191456.1:n.376-59_376-57dup
NM_006280.3:c.352-59_352-57dup MANE Select	NP_006271.1:n.352-59_352-57dup