Canonical Allele Identifier: CA2466480567

Gene: SSR4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.386C= MANE Select	ENSP00000359103.3:p.Pro129=
ENST00000320857.7:c.386C=	ENSP00000317331.3:p.Pro129=
ENST00000370085.3:c.311C=	ENSP00000359102.3:p.Pro104=
ENST00000370086.7:c.386C=	ENSP00000359103.3:p.Pro129=
ENST00000370087.5:c.386C=	ENSP00000359104.1:p.Pro129=
ENST00000447375.1:n.226C=
ENST00000460616.5:n.2094C=
ENST00000471880.5:n.589C=
ENST00000482902.5:n.2213C=
ENST00000485612.5:n.501C=
ENST00000486204.5:n.458C=
NM_001204526.1:c.419C=	NP_001191455.1:p.Pro140=
NM_001204527.1:c.410C=	NP_001191456.1:p.Pro137=
NM_006280.2:c.386C=	NP_006271.1:p.Pro129=
NR_037927.1:n.731C=
XM_011531186.1:c.386C=	XP_011529488.1:p.Pro129=
XM_011531187.1:c.386C=	XP_011529489.1:p.Pro129=
XM_017029756.1:c.197C=	XP_016885245.1:p.Pro66=
XM_017029757.1:c.197C=	XP_016885246.1:p.Pro66=
XM_024452428.1:c.197C=	XP_024308196.1:p.Pro66=
NM_001204527.2:c.410C=	NP_001191456.1:p.Pro137=
NM_006280.3:c.386C= MANE Select	NP_006271.1:p.Pro129=