Canonical Allele Identifier: CA2494338158

Gene: CAMKMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44541063T= , CM000664.2:g.44541063T=	GRCh38
NC_000002.11:g.44768202T= , CM000664.1:g.44768202T=	GRCh37
NC_000002.10:g.44621706T=	NCBI36
NG_032944.1:g.184160T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378494.8:c.376+150758T= MANE Select	ENSP00000367755.3:n.376+150758T=
ENST00000378494.7:c.376+150758T=	ENSP00000367755.3:n.376+150758T=
ENST00000402247.5:c.377-8492T=	ENSP00000385587.1:n.377-8492T=
ENST00000407131.5:c.377-90428T=	ENSP00000384039.1:n.377-90428T=
ENST00000428993.1:c.207-8492T=
NM_024766.4:c.376+150758T=	NP_079042.1:n.376+150758T=
XM_011533111.1:c.376+150758T=	XP_011531413.1:n.376+150758T=
XM_011533112.1:c.376+150758T=	XP_011531414.1:n.376+150758T=
XR_939721.1:n.446+150758T=
XR_939722.1:n.446+150758T=
XR_939723.1:n.446+150758T=
XM_011533111.2:c.376+150758T=	XP_011531413.1:n.376+150758T=
XM_017004971.1:c.662-16825T=	XP_016860460.1:n.662-16825T=
XM_017004982.2:c.4+35333T=	XP_016860471.1:n.4+35333T=
XM_017004983.2:c.4+35333T=	XP_016860472.1:n.4+35333T=
XR_001738949.2:n.446+150758T=
XR_001738950.1:n.670+150758T=
XR_939722.2:n.446+150758T=
NM_024766.5:c.376+150758T= MANE Select	NP_079042.1:n.376+150758T=