Canonical Allele Identifier: CA519232670

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063564T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798109T>G , CM000685.2:g.153798109T>G	GRCh38
NC_000023.10:g.153063564T>G , CM000685.1:g.153063564T>G	GRCh37
NC_000023.9:g.152716758T>G	NCBI36
NG_041795.1:g.8935T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.390T>G MANE Select	ENSP00000359103.3:p.Pro130=
ENST00000320857.7:c.390T>G	ENSP00000317331.3:p.Pro130=
ENST00000370085.3:c.315T>G	ENSP00000359102.3:p.Pro105=
ENST00000370086.7:c.390T>G	ENSP00000359103.3:p.Pro130=
ENST00000370087.5:c.390T>G	ENSP00000359104.1:p.Pro130=
ENST00000447375.1:n.230T>G
ENST00000460616.5:n.2098T>G
ENST00000471880.5:n.593T>G
ENST00000482902.5:n.2217T>G
ENST00000485612.5:n.505T>G
ENST00000486204.5:n.462T>G
NM_001204526.1:c.423T>G	NP_001191455.1:p.Pro141=
NM_001204527.1:c.414T>G	NP_001191456.1:p.Pro138=
NM_006280.2:c.390T>G	NP_006271.1:p.Pro130=
NR_037927.1:n.735T>G
XM_011531186.1:c.390T>G	XP_011529488.1:p.Pro130=
XM_011531187.1:c.390T>G	XP_011529489.1:p.Pro130=
XM_017029756.1:c.201T>G	XP_016885245.1:p.Pro67=
XM_017029757.1:c.201T>G	XP_016885246.1:p.Pro67=
XM_024452428.1:c.201T>G	XP_024308196.1:p.Pro67=
NM_001204527.2:c.414T>G	NP_001191456.1:p.Pro138=
NM_006280.3:c.390T>G MANE Select	NP_006271.1:p.Pro130=