Canonical Allele Identifier: CA415186967

Gene: SSR4

Linked Data

• MyVariant Identifiers: chrX:g.153063536A>C (hg19) ; chrX:g.153798081A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798081A>C , CM000685.2:g.153798081A>C	GRCh38
NC_000023.10:g.153063536A>C , CM000685.1:g.153063536A>C	GRCh37
NC_000023.9:g.152716730A>C	NCBI36
NG_041795.1:g.8907A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.362A>C MANE Select	ENSP00000359103.3:p.Asn121Thr
ENST00000320857.7:c.362A>C	ENSP00000317331.3:p.Asn121Thr
ENST00000370085.3:c.287A>C	ENSP00000359102.3:p.Asn96Thr
ENST00000370086.7:c.362A>C	ENSP00000359103.3:p.Asn121Thr
ENST00000370087.5:c.362A>C	ENSP00000359104.1:p.Asn121Thr
ENST00000447375.1:n.202A>C
ENST00000460616.5:n.2070A>C
ENST00000471880.5:n.565A>C
ENST00000482902.5:n.2189A>C
ENST00000485612.5:n.477A>C
ENST00000486204.5:n.434A>C
NM_001204526.1:c.395A>C	NP_001191455.1:p.Asn132Thr
NM_001204527.1:c.386A>C	NP_001191456.1:p.Asn129Thr
NM_006280.2:c.362A>C	NP_006271.1:p.Asn121Thr
NR_037927.1:n.707A>C
XM_011531186.1:c.362A>C	XP_011529488.1:p.Asn121Thr
XM_011531187.1:c.362A>C	XP_011529489.1:p.Asn121Thr
XM_017029756.1:c.173A>C	XP_016885245.1:p.Asn58Thr
XM_017029757.1:c.173A>C	XP_016885246.1:p.Asn58Thr
XM_024452428.1:c.173A>C	XP_024308196.1:p.Asn58Thr
NM_001204527.2:c.386A>C	NP_001191456.1:p.Asn129Thr
NM_006280.3:c.362A>C MANE Select	NP_006271.1:p.Asn121Thr