Canonical Allele Identifier: CA415187115

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063586C>T (hg19) ; chrX:g.153798131C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798131C>T , CM000685.2:g.153798131C>T	GRCh38
NC_000023.10:g.153063586C>T , CM000685.1:g.153063586C>T	GRCh37
NC_000023.9:g.152716780C>T	NCBI36
NG_041795.1:g.8957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.412C>T MANE Select	ENSP00000359103.3:p.His138Tyr
ENST00000320857.7:c.412C>T	ENSP00000317331.3:p.His138Tyr
ENST00000370085.3:c.337C>T	ENSP00000359102.3:p.His113Tyr
ENST00000370086.7:c.412C>T	ENSP00000359103.3:p.His138Tyr
ENST00000370087.5:c.412C>T	ENSP00000359104.1:p.His138Tyr
ENST00000447375.1:n.252C>T
ENST00000460616.5:n.2120C>T
ENST00000471880.5:n.615C>T
ENST00000482902.5:n.2239C>T
ENST00000485612.5:n.527C>T
ENST00000486204.5:n.484C>T
NM_001204526.1:c.445C>T	NP_001191455.1:p.His149Tyr
NM_001204527.1:c.436C>T	NP_001191456.1:p.His146Tyr
NM_006280.2:c.412C>T	NP_006271.1:p.His138Tyr
NR_037927.1:n.757C>T
XM_011531186.1:c.412C>T	XP_011529488.1:p.His138Tyr
XM_011531187.1:c.412C>T	XP_011529489.1:p.His138Tyr
XM_017029756.1:c.223C>T	XP_016885245.1:p.His75Tyr
XM_017029757.1:c.223C>T	XP_016885246.1:p.His75Tyr
XM_024452428.1:c.223C>T	XP_024308196.1:p.His75Tyr
NM_001204527.2:c.436C>T	NP_001191456.1:p.His146Tyr
NM_006280.3:c.412C>T MANE Select	NP_006271.1:p.His138Tyr