Canonical Allele Identifier: CA1160114012

Gene: RPS6KA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26539458_26539459delinsCA , CM000663.2:g.26539458_26539459delinsCA	GRCh38
NC_000001.10:g.26865949_26865950delinsCA , CM000663.1:g.26865949_26865950delinsCA	GRCh37
NC_000001.9:g.26738536_26738537delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374168.7:c.108+2489_108+2490delinsCA MANE Select	ENSP00000363283.2:n.108+2489_108+2490deli...
ENST00000374166.8:c.108+2489_108+2490delinsCA	ENSP00000363281.4:n.108+2489_108+2490deli...
ENST00000374168.6:c.108+2489_108+2490delinsCA	ENSP00000363283.2:n.108+2489_108+2490deli...
ENST00000524436.5:n.254+2489_254+2490delinsCA
ENST00000525525.5:c.*95+2489_*95+2490delinsCA	ENSP00000434616.1:n.*95+2489_*95+2490deli...
ENST00000526040.6:c.108+2489_108+2490delinsCA	ENSP00000436990.1:n.108+2489_108+2490deli...
ENST00000526792.5:c.-169+2489_-169+2490delinsCA	ENSP00000431651.1:n.-169+2489_-169+2490de...
ENST00000529454.5:c.-52+2489_-52+2490delinsCA	ENSP00000433039.1:n.-52+2489_-52+2490deli...
NM_002953.3:c.108+2489_108+2490delinsCA	NP_002944.2:n.108+2489_108+2490delinsCA
XM_005245967.2:c.-169+2489_-169+2490delinsCA	XP_005246024.1:n.-169+2489_-169+2490delin...
XM_011541898.1:c.-169+2489_-169+2490delinsCA	XP_011540200.1:n.-169+2489_-169+2490delin...
XM_024448871.1:c.-169+2489_-169+2490delinsCA	XP_024304639.1:n.-169+2489_-169+2490delin...
NM_002953.4:c.108+2489_108+2490delinsCA MANE Select	NP_002944.2:n.108+2489_108+2490delinsCA