Canonical Allele Identifier: CA223830248

Gene: RPS6KA4

Linked Data

• dbSNP Id: rs554944956
• gnomAD v3: 11-64367734-A-C
• gnomAD v4: 11-64367734-A-C
• MyVariant Identifiers: chr11:g.64135206A>C (hg19) ; chr11:g.64367734A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64367734A>C , CM000673.2:g.64367734A>C	GRCh38
NC_000011.9:g.64135206A>C , CM000673.1:g.64135206A>C	GRCh37
NC_000011.8:g.63891782A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334205.9:c.1072-398A>C MANE Select	ENSP00000333896.4:n.1072-398A>C
ENST00000334205.8:c.1072-398A>C	ENSP00000333896.4:n.1072-398A>C
ENST00000528057.5:c.1072-398A>C	ENSP00000435580.1:n.1072-398A>C
ENST00000528355.5:c.*879-398A>C	ENSP00000435314.1:n.*879-398A>C
ENST00000530504.1:c.1024-398A>C	ENSP00000432945.1:n.1024-398A>C
ENST00000532885.5:n.631-398A>C
NM_001006944.1:c.1072-398A>C	NP_001006945.1:n.1072-398A>C
NM_001300802.1:c.1072-398A>C	NP_001287731.1:n.1072-398A>C
NM_003942.2:c.1072-398A>C	NP_003933.1:n.1072-398A>C
XM_005274380.1:c.907-398A>C	XP_005274437.1:n.907-398A>C
XM_005274381.3:c.883-398A>C	XP_005274438.1:n.883-398A>C
NM_001318361.1:c.883-398A>C	NP_001305290.1:n.883-398A>C
XM_017018527.2:c.-51-398A>C	XP_016874016.1:n.-51-398A>C
NM_003942.3:c.1072-398A>C MANE Select	NP_003933.1:n.1072-398A>C
NM_001006944.2:c.1072-398A>C	NP_001006945.1:n.1072-398A>C
NM_001300802.2:c.1072-398A>C	NP_001287731.1:n.1072-398A>C
NM_001318361.2:c.883-398A>C	NP_001305290.1:n.883-398A>C