Canonical Allele Identifier: CA415187016

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063557T>G (hg19) ; chrX:g.153798102T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798102T>G , CM000685.2:g.153798102T>G	GRCh38
NC_000023.10:g.153063557T>G , CM000685.1:g.153063557T>G	GRCh37
NC_000023.9:g.152716751T>G	NCBI36
NG_041795.1:g.8928T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.383T>G MANE Select	ENSP00000359103.3:p.Ile128Ser
ENST00000320857.7:c.383T>G	ENSP00000317331.3:p.Ile128Ser
ENST00000370085.3:c.308T>G	ENSP00000359102.3:p.Ile103Ser
ENST00000370086.7:c.383T>G	ENSP00000359103.3:p.Ile128Ser
ENST00000370087.5:c.383T>G	ENSP00000359104.1:p.Ile128Ser
ENST00000447375.1:n.223T>G
ENST00000460616.5:n.2091T>G
ENST00000471880.5:n.586T>G
ENST00000482902.5:n.2210T>G
ENST00000485612.5:n.498T>G
ENST00000486204.5:n.455T>G
NM_001204526.1:c.416T>G	NP_001191455.1:p.Ile139Ser
NM_001204527.1:c.407T>G	NP_001191456.1:p.Ile136Ser
NM_006280.2:c.383T>G	NP_006271.1:p.Ile128Ser
NR_037927.1:n.728T>G
XM_011531186.1:c.383T>G	XP_011529488.1:p.Ile128Ser
XM_011531187.1:c.383T>G	XP_011529489.1:p.Ile128Ser
XM_017029756.1:c.194T>G	XP_016885245.1:p.Ile65Ser
XM_017029757.1:c.194T>G	XP_016885246.1:p.Ile65Ser
XM_024452428.1:c.194T>G	XP_024308196.1:p.Ile65Ser
NM_001204527.2:c.407T>G	NP_001191456.1:p.Ile136Ser
NM_006280.3:c.383T>G MANE Select	NP_006271.1:p.Ile128Ser