Canonical Allele Identifier: CA519232782

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063582G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798127G>T , CM000685.2:g.153798127G>T	GRCh38
NC_000023.10:g.153063582G>T , CM000685.1:g.153063582G>T	GRCh37
NC_000023.9:g.152716776G>T	NCBI36
NG_041795.1:g.8953G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.408G>T MANE Select	ENSP00000359103.3:p.Val136=
ENST00000320857.7:c.408G>T	ENSP00000317331.3:p.Val136=
ENST00000370085.3:c.333G>T	ENSP00000359102.3:p.Val111=
ENST00000370086.7:c.408G>T	ENSP00000359103.3:p.Val136=
ENST00000370087.5:c.408G>T	ENSP00000359104.1:p.Val136=
ENST00000447375.1:n.248G>T
ENST00000460616.5:n.2116G>T
ENST00000471880.5:n.611G>T
ENST00000482902.5:n.2235G>T
ENST00000485612.5:n.523G>T
ENST00000486204.5:n.480G>T
NM_001204526.1:c.441G>T	NP_001191455.1:p.Val147=
NM_001204527.1:c.432G>T	NP_001191456.1:p.Val144=
NM_006280.2:c.408G>T	NP_006271.1:p.Val136=
NR_037927.1:n.753G>T
XM_011531186.1:c.408G>T	XP_011529488.1:p.Val136=
XM_011531187.1:c.408G>T	XP_011529489.1:p.Val136=
XM_017029756.1:c.219G>T	XP_016885245.1:p.Val73=
XM_017029757.1:c.219G>T	XP_016885246.1:p.Val73=
XM_024452428.1:c.219G>T	XP_024308196.1:p.Val73=
NM_001204527.2:c.432G>T	NP_001191456.1:p.Val144=
NM_006280.3:c.408G>T MANE Select	NP_006271.1:p.Val136=