Canonical Allele Identifier: CA1160114010

Gene: RPS6KA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26539456_26539457delinsTG , CM000663.2:g.26539456_26539457delinsTG	GRCh38
NC_000001.10:g.26865947_26865948delinsTG , CM000663.1:g.26865947_26865948delinsTG	GRCh37
NC_000001.9:g.26738534_26738535delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374168.7:c.108+2487_108+2488delinsTG MANE Select	ENSP00000363283.2:n.108+2487_108+2488deli...
ENST00000374166.8:c.108+2487_108+2488delinsTG	ENSP00000363281.4:n.108+2487_108+2488deli...
ENST00000374168.6:c.108+2487_108+2488delinsTG	ENSP00000363283.2:n.108+2487_108+2488deli...
ENST00000524436.5:n.254+2487_254+2488delinsTG
ENST00000525525.5:c.*95+2487_*95+2488delinsTG	ENSP00000434616.1:n.*95+2487_*95+2488deli...
ENST00000526040.6:c.108+2487_108+2488delinsTG	ENSP00000436990.1:n.108+2487_108+2488deli...
ENST00000526792.5:c.-169+2487_-169+2488delinsTG	ENSP00000431651.1:n.-169+2487_-169+2488de...
ENST00000529454.5:c.-52+2487_-52+2488delinsTG	ENSP00000433039.1:n.-52+2487_-52+2488deli...
NM_002953.3:c.108+2487_108+2488delinsTG	NP_002944.2:n.108+2487_108+2488delinsTG
XM_005245967.2:c.-169+2487_-169+2488delinsTG	XP_005246024.1:n.-169+2487_-169+2488delin...
XM_011541898.1:c.-169+2487_-169+2488delinsTG	XP_011540200.1:n.-169+2487_-169+2488delin...
XM_024448871.1:c.-169+2487_-169+2488delinsTG	XP_024304639.1:n.-169+2487_-169+2488delin...
NM_002953.4:c.108+2487_108+2488delinsTG MANE Select	NP_002944.2:n.108+2487_108+2488delinsTG