Canonical Allele Identifier: CA415187022

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063560C>A (hg19) ; chrX:g.153798105C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798105C>A , CM000685.2:g.153798105C>A	GRCh38
NC_000023.10:g.153063560C>A , CM000685.1:g.153063560C>A	GRCh37
NC_000023.9:g.152716754C>A	NCBI36
NG_041795.1:g.8931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.386C>A MANE Select	ENSP00000359103.3:p.Pro129Gln
ENST00000320857.7:c.386C>A	ENSP00000317331.3:p.Pro129Gln
ENST00000370085.3:c.311C>A	ENSP00000359102.3:p.Pro104Gln
ENST00000370086.7:c.386C>A	ENSP00000359103.3:p.Pro129Gln
ENST00000370087.5:c.386C>A	ENSP00000359104.1:p.Pro129Gln
ENST00000447375.1:n.226C>A
ENST00000460616.5:n.2094C>A
ENST00000471880.5:n.589C>A
ENST00000482902.5:n.2213C>A
ENST00000485612.5:n.501C>A
ENST00000486204.5:n.458C>A
NM_001204526.1:c.419C>A	NP_001191455.1:p.Pro140Gln
NM_001204527.1:c.410C>A	NP_001191456.1:p.Pro137Gln
NM_006280.2:c.386C>A	NP_006271.1:p.Pro129Gln
NR_037927.1:n.731C>A
XM_011531186.1:c.386C>A	XP_011529488.1:p.Pro129Gln
XM_011531187.1:c.386C>A	XP_011529489.1:p.Pro129Gln
XM_017029756.1:c.197C>A	XP_016885245.1:p.Pro66Gln
XM_017029757.1:c.197C>A	XP_016885246.1:p.Pro66Gln
XM_024452428.1:c.197C>A	XP_024308196.1:p.Pro66Gln
NM_001204527.2:c.410C>A	NP_001191456.1:p.Pro137Gln
NM_006280.3:c.386C>A MANE Select	NP_006271.1:p.Pro129Gln