Canonical Allele Identifier: CA2138318799

Gene: SOCS4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55031230G= , CM000676.2:g.55031230G=	GRCh38
NC_000014.8:g.55497948G= , CM000676.1:g.55497948G=	GRCh37
NC_000014.7:g.54567698G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_199421.2:c.-219-633G= MANE Select	NP_955453.1:n.-219-633G=
ENST00000555846.2:c.-219-633G= MANE Select	ENSP00000452522.1:n.-219-633G=
NM_080867.2:c.-91+3759G=	NP_543143.1:n.-91+3759G=
NM_080867.3:c.-91+3759G=	NP_543143.1:n.-91+3759G=
NM_199421.1:c.-219-633G=	NP_955453.1:n.-219-633G=
ENST00000339298.2:c.-91+3472G=	ENSP00000341327.2:n.-91+3472G=
ENST00000395472.2:c.-91+3759G=	ENSP00000378855.2:n.-91+3759G=
ENST00000553735.1:n.192-659G=
ENST00000555846.1:c.-219-633G=	ENSP00000452522.1:n.-219-633G=
XM_011536425.1:c.-278-574G=	XP_011534727.1:n.-278-574G=
XM_011536426.1:c.-193-659G=	XP_011534728.1:n.-193-659G=