Canonical Allele Identifier: CA519231801

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063528T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798073T>G , CM000685.2:g.153798073T>G	GRCh38
NC_000023.10:g.153063528T>G , CM000685.1:g.153063528T>G	GRCh37
NC_000023.9:g.152716722T>G	NCBI36
NG_041795.1:g.8899T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.354T>G MANE Select	ENSP00000359103.3:p.Ala118=
ENST00000320857.7:c.354T>G	ENSP00000317331.3:p.Ala118=
ENST00000370085.3:c.279T>G	ENSP00000359102.3:p.Ala93=
ENST00000370086.7:c.354T>G	ENSP00000359103.3:p.Ala118=
ENST00000370087.5:c.354T>G	ENSP00000359104.1:p.Ala118=
ENST00000447375.1:n.194T>G
ENST00000460616.5:n.2062T>G
ENST00000471880.5:n.557T>G
ENST00000482902.5:n.2181T>G
ENST00000485612.5:n.469T>G
ENST00000486204.5:n.426T>G
NM_001204526.1:c.387T>G	NP_001191455.1:p.Ala129=
NM_001204527.1:c.378T>G	NP_001191456.1:p.Ala126=
NM_006280.2:c.354T>G	NP_006271.1:p.Ala118=
NR_037927.1:n.699T>G
XM_011531186.1:c.354T>G	XP_011529488.1:p.Ala118=
XM_011531187.1:c.354T>G	XP_011529489.1:p.Ala118=
XM_017029756.1:c.165T>G	XP_016885245.1:p.Ala55=
XM_017029757.1:c.165T>G	XP_016885246.1:p.Ala55=
XM_024452428.1:c.165T>G	XP_024308196.1:p.Ala55=
NM_001204527.2:c.378T>G	NP_001191456.1:p.Ala126=
NM_006280.3:c.354T>G MANE Select	NP_006271.1:p.Ala118=