Canonical Allele Identifier: CA290148397

Gene: SOCS7

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.38393251T>A , CM000679.2:g.38393251T>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612932.6:c.1682-2058T>A MANE Select	ENSP00000482229.2:n.1682-2058T>A
ENST00000613678.5:c.1405-2058T>A
ENST00000665913.1:c.1490-2058T>A	ENSP00000499750.1:n.1490-2058T>A
ENST00000612932.4:c.1490-2058T>A	ENSP00000482229.1:n.1490-2058T>A
ENST00000613678.4:c.1388-2058T>A	ENSP00000484381.1:n.1388-2058T>A
ENST00000617360.1:n.1931-6262T>A
NM_014598.3:c.1490-2058T>A	NP_055413.1:n.1490-2058T>A
XM_017024551.1:c.1580-2058T>A	XP_016880040.1:n.1580-2058T>A
XM_017024552.1:c.1475-2058T>A	XP_016880041.1:n.1475-2058T>A
XR_001752503.1:n.2051-2058T>A
NM_014598.4:c.1682-2058T>A MANE Select	NP_055413.2:n.1682-2058T>A