Canonical Allele Identifier: CA1160114054

Gene: RPS6KA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26539559_26539560delinsAG , CM000663.2:g.26539559_26539560delinsAG	GRCh38
NC_000001.10:g.26866050_26866051delinsAG , CM000663.1:g.26866050_26866051delinsAG	GRCh37
NC_000001.9:g.26738637_26738638delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374168.7:c.108+2590_108+2591delinsAG MANE Select	ENSP00000363283.2:n.108+2590_108+2591delinsAG
ENST00000374166.8:c.108+2590_108+2591delinsAG	ENSP00000363281.4:n.108+2590_108+2591delinsAG
ENST00000374168.6:c.108+2590_108+2591delinsAG	ENSP00000363283.2:n.108+2590_108+2591delinsAG
ENST00000524436.5:n.254+2590_254+2591delinsAG
ENST00000525525.5:c.*95+2590_*95+2591delinsAG	ENSP00000434616.1:n.*95+2590_*95+2591delinsAG
ENST00000526040.6:c.108+2590_108+2591delinsAG	ENSP00000436990.1:n.108+2590_108+2591delinsAG
ENST00000526792.5:c.-169+2590_-169+2591delinsAG	ENSP00000431651.1:n.-169+2590_-169+2591delinsAG
ENST00000529454.5:c.-52+2590_-52+2591delinsAG	ENSP00000433039.1:n.-52+2590_-52+2591delinsAG
NM_002953.3:c.108+2590_108+2591delinsAG	NP_002944.2:n.108+2590_108+2591delinsAG
XM_005245967.2:c.-169+2590_-169+2591delinsAG	XP_005246024.1:n.-169+2590_-169+2591delinsAG
XM_011541898.1:c.-169+2590_-169+2591delinsAG	XP_011540200.1:n.-169+2590_-169+2591delinsAG
XM_024448871.1:c.-169+2590_-169+2591delinsAG	XP_024304639.1:n.-169+2590_-169+2591delinsAG
NM_002953.4:c.108+2590_108+2591delinsAG MANE Select	NP_002944.2:n.108+2590_108+2591delinsAG