Canonical Allele Identifier: CA12219035

Gene: RPS6KA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166763934G>A , CM000668.2:g.166763934G>A	GRCh38
NC_000006.11:g.167177422G>A , CM000668.1:g.167177422G>A	GRCh37
NC_000006.10:g.167097412G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503859.5:c.123+94266C>T	ENSP00000427015.1:n.123+94266C>T
ENST00000506565.1:c.174+6929C>T	ENSP00000425148.1:n.174+6929C>T
ENST00000510118.5:c.174+6929C>T	ENSP00000422435.1:n.174+6929C>T
ENST00000512860.5:c.-169+142424C>T	ENSP00000427605.1:n.-169+142424C>T
NM_001006932.1:c.123+94266C>T	NP_001006933.1:n.123+94266C>T
XM_005267092.2:c.174+6929C>T	XP_005267149.1:n.174+6929C>T
XM_011536059.1:c.174+6929C>T	XP_011534361.1:n.174+6929C>T
XM_011536060.1:c.93+6929C>T	XP_011534362.1:n.93+6929C>T
XM_011536061.1:c.93+6929C>T	XP_011534363.1:n.93+6929C>T
NM_001006932.2:c.123+94266C>T	NP_001006933.2:n.123+94266C>T
NM_001318936.1:c.174+6929C>T	NP_001305865.1:n.174+6929C>T
NM_001318937.1:c.37+98174C>T	NP_001305866.1:n.37+98174C>T
NM_001006932.3:c.123+94266C>T	NP_001006933.3:n.123+94266C>T
NM_001318936.2:c.174+6929C>T	NP_001305865.2:n.174+6929C>T
NM_001318937.2:c.37+98174C>T	NP_001305866.1:n.37+98174C>T