Canonical Allele Identifier: CA6834614

Gene: CAMKK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121253327G>A , CM000674.2:g.121253327G>A	GRCh38
NC_000012.11:g.121691130G>A , CM000674.1:g.121691130G>A	GRCh37
NC_000012.10:g.120175513G>A	NCBI36
NG_029409.1:g.49982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404169.8:c.1053C>T MANE Select	ENSP00000384600.3:p.Pro351=
ENST00000652382.1:c.1053C>T	ENSP00000498824.1:p.Pro351=
ENST00000324774.9:c.1053C>T	ENSP00000312741.5:p.Pro351=
ENST00000337174.7:c.1053C>T	ENSP00000336634.3:p.Pro351=
ENST00000347034.6:c.1053C>T	ENSP00000321230.3:p.Pro351=
ENST00000392473.2:c.1053C>T	ENSP00000376265.2:p.Pro351=
ENST00000392474.6:c.1053C>T	ENSP00000376266.2:p.Pro351=
ENST00000402834.8:c.1053C>T	ENSP00000384591.4:p.Pro351=
ENST00000404169.7:c.1053C>T	ENSP00000384600.3:p.Pro351=
ENST00000412367.6:c.1053C>T	ENSP00000388368.2:p.Pro351=
ENST00000446440.6:c.1053C>T	ENSP00000388273.2:p.Pro351=
ENST00000535524.1:n.743C>T
ENST00000538733.5:c.1053C>T	ENSP00000445944.1:p.Pro351=
ENST00000545538.5:c.414C>T	ENSP00000441352.1:p.Pro138=
NM_001270485.1:c.1053C>T	NP_001257414.1:p.Pro351=
NM_001270486.1:c.1053C>T	NP_001257415.1:p.Pro351=
NM_006549.3:c.1053C>T	NP_006540.3:p.Pro351=
NM_153499.2:c.1053C>T	NP_705719.2:p.Pro351=
NM_153500.1:c.1053C>T	NP_705720.1:p.Pro351=
NM_172214.2:c.1053C>T	NP_757363.1:p.Pro351=
NM_172215.2:c.1053C>T	NP_757364.1:p.Pro351=
NM_172216.1:c.1053C>T	NP_757365.1:p.Pro351=
NM_172226.2:c.1053C>T	NP_757380.1:p.Pro351=
XM_005253822.3:c.1053C>T	XP_005253879.1:p.Pro351=
XM_005253823.1:c.1053C>T	XP_005253880.1:p.Pro351=
XM_005253824.3:c.1053C>T	XP_005253881.1:p.Pro351=
XM_011537762.1:c.1053C>T	XP_011536064.1:p.Pro351=
XM_011537763.1:c.1053C>T	XP_011536065.1:p.Pro351=
XM_011537764.1:c.561C>T	XP_011536066.1:p.Pro187=
XM_011537765.1:c.228C>T	XP_011536067.1:p.Pro76=
XM_011537764.2:c.561C>T	XP_011536066.1:p.Pro187=
XM_017018694.1:c.1107C>T	XP_016874183.1:p.Pro369=
XM_017018695.1:c.1107C>T	XP_016874184.1:p.Pro369=
XM_017018699.1:c.1107C>T	XP_016874188.1:p.Pro369=
XM_017018700.1:c.1107C>T	XP_016874189.1:p.Pro369=
XM_017018702.2:c.1053C>T	XP_016874191.1:p.Pro351=
XM_017018703.1:c.1107C>T	XP_016874192.1:p.Pro369=
XM_017018705.1:c.1107C>T	XP_016874194.1:p.Pro369=
XM_017018706.1:c.561C>T	XP_016874195.1:p.Pro187=
XM_017018708.1:c.561C>T	XP_016874197.1:p.Pro187=
XM_017018709.2:c.228C>T	XP_016874198.1:p.Pro76=
XM_024448798.1:c.561C>T	XP_024304566.1:p.Pro187=
XM_024448799.1:c.228C>T	XP_024304567.1:p.Pro76=
XR_001748557.1:n.1201C>T
XR_001748558.1:n.1201C>T
NM_001270485.2:c.1053C>T MANE Select	NP_001257414.1:p.Pro351=
NM_172214.3:c.1053C>T	NP_757363.1:p.Pro351=
NM_172215.3:c.1053C>T	NP_757364.1:p.Pro351=
NM_006549.4:c.1053C>T	NP_006540.3:p.Pro351=
NM_153499.3:c.1053C>T	NP_705719.2:p.Pro351=
NM_153500.2:c.1053C>T	NP_705720.1:p.Pro351=
NM_172216.2:c.1053C>T	NP_757365.1:p.Pro351=
NM_172226.3:c.1053C>T	NP_757380.1:p.Pro351=