Canonical Allele Identifier: CA12250464

Gene: IL20RA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137027888A>G , CM000668.2:g.137027888A>G	GRCh38
NC_000006.11:g.137349025A>G , CM000668.1:g.137349025A>G	GRCh37
NC_000006.10:g.137390718A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316649.10:c.89-10785T>C MANE Select	ENSP00000314976.5:n.89-10785T>C
ENST00000316649.9:c.89-10785T>C	ENSP00000314976.5:n.89-10785T>C
ENST00000367746.3:c.89-10785T>C	ENSP00000356720.3:n.89-10785T>C
ENST00000367748.4:c.-66-10785T>C	ENSP00000356722.1:n.-66-10785T>C
ENST00000468393.5:c.-66-10785T>C	ENSP00000489177.1:n.-66-10785T>C
ENST00000541547.5:c.-59-10785T>C	ENSP00000437843.1:n.-59-10785T>C
ENST00000635289.1:c.-66-10785T>C	ENSP00000489419.1:n.-66-10785T>C
NM_001278722.1:c.-59-10785T>C	NP_001265651.1:n.-59-10785T>C
NM_001278723.1:c.-66-10785T>C	NP_001265652.1:n.-66-10785T>C
NM_001278724.1:c.-66-10785T>C	NP_001265653.1:n.-66-10785T>C
NM_014432.3:c.89-10785T>C	NP_055247.3:n.89-10785T>C
XM_006715505.2:c.89-10785T>C	XP_006715568.1:n.89-10785T>C
XM_006715506.2:c.-66-10785T>C	XP_006715569.1:n.-66-10785T>C
XM_011535904.1:c.-66-10785T>C	XP_011534206.1:n.-66-10785T>C
XM_011535904.2:c.-66-10785T>C	XP_011534206.1:n.-66-10785T>C
XM_017010954.2:c.89-10785T>C	XP_016866443.1:n.89-10785T>C
XM_017010955.1:c.-59-10785T>C	XP_016866444.1:n.-59-10785T>C
NM_001278724.2:c.-66-10785T>C	NP_001265653.2:n.-66-10785T>C
NM_001278722.2:c.-59-10785T>C	NP_001265651.2:n.-59-10785T>C
NM_001278723.3:c.-66-10785T>C	NP_001265652.2:n.-66-10785T>C
NM_001278724.4:c.-66-10785T>C	NP_001265653.2:n.-66-10785T>C
NM_014432.4:c.89-10785T>C MANE Select	NP_055247.4:n.89-10785T>C