Canonical Allele Identifier: CA223830253

Gene: RPS6KA4

Linked Data

• dbSNP Id: rs1025342213
• gnomAD v2: 11-64135208-G-A
• gnomAD v3: 11-64367736-G-A
• gnomAD v4: 11-64367736-G-A
• MyVariant Identifiers: chr11:g.64135208G>A (hg19) ; chr11:g.64367736G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64367736G>A , CM000673.2:g.64367736G>A	GRCh38
NC_000011.9:g.64135208G>A , CM000673.1:g.64135208G>A	GRCh37
NC_000011.8:g.63891784G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334205.9:c.1072-396G>A MANE Select	ENSP00000333896.4:n.1072-396G>A
ENST00000334205.8:c.1072-396G>A	ENSP00000333896.4:n.1072-396G>A
ENST00000528057.5:c.1072-396G>A	ENSP00000435580.1:n.1072-396G>A
ENST00000528355.5:c.*879-396G>A	ENSP00000435314.1:n.*879-396G>A
ENST00000530504.1:c.1024-396G>A	ENSP00000432945.1:n.1024-396G>A
ENST00000532885.5:n.631-396G>A
NM_001006944.1:c.1072-396G>A	NP_001006945.1:n.1072-396G>A
NM_001300802.1:c.1072-396G>A	NP_001287731.1:n.1072-396G>A
NM_003942.2:c.1072-396G>A	NP_003933.1:n.1072-396G>A
XM_005274380.1:c.907-396G>A	XP_005274437.1:n.907-396G>A
XM_005274381.3:c.883-396G>A	XP_005274438.1:n.883-396G>A
NM_001318361.1:c.883-396G>A	NP_001305290.1:n.883-396G>A
XM_017018527.2:c.-51-396G>A	XP_016874016.1:n.-51-396G>A
NM_003942.3:c.1072-396G>A MANE Select	NP_003933.1:n.1072-396G>A
NM_001006944.2:c.1072-396G>A	NP_001006945.1:n.1072-396G>A
NM_001300802.2:c.1072-396G>A	NP_001287731.1:n.1072-396G>A
NM_001318361.2:c.883-396G>A	NP_001305290.1:n.883-396G>A