Canonical Allele Identifier: CA2068752029

Gene: MTRFR CDK2AP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123257037G= , CM000674.2:g.123257037G=	GRCh38
NC_000012.11:g.123741584G= , CM000674.1:g.123741584G=	GRCh37
NC_000012.10:g.122307537G=	NCBI36
NG_027517.1:g.28741G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253233.6:c.*6G= (MTRFR) MANE Select	ENSP00000253233.1:n.*6G=
ENST00000366329.7:c.*6G= (MTRFR)	ENSP00000390647.1:n.*6G=
ENST00000425637.3:c.*1224G= (MTRFR)	ENSP00000506680.1:n.*1224G=
ENST00000536130.2:c.*6G= (MTRFR)	ENSP00000443072.2:n.*6G=
ENST00000538888.6:c.*390G= (MTRFR)	ENSP00000505059.1:n.*390G=
ENST00000541002.7:n.809+2006C=
ENST00000543217.6:n.280+2006C=
ENST00000652466.1:c.*955+3237C= (CDK2AP1)	ENSP00000498286.1:n.*955+3237C=
ENST00000679849.1:c.*6G= (MTRFR)	ENSP00000505808.1:n.*6G=
ENST00000680325.1:c.*895G= (MTRFR)	ENSP00000505277.1:n.*895G=
ENST00000253233.5:c.*6G= (MTRFR)	ENSP00000253233.1:n.*6G=
ENST00000366329.6:c.*6G= (MTRFR)	ENSP00000390647.1:n.*6G=
ENST00000429587.2:c.*6G= (MTRFR)	ENSP00000391513.2:n.*6G=
NM_001143905.2:c.*6G= (MTRFR)	NP_001137377.1:n.*6G=
NM_001194995.1:c.*6G= (MTRFR)	NP_001181924.1:n.*6G=
NM_152269.4:c.*6G= (MTRFR)	NP_689482.1:n.*6G=
XM_005253630.3:c.*6G= (MTRFR)	XP_005253687.1:n.*6G=
XM_011538980.1:c.*6G= (MTRFR)	XP_011537282.1:n.*6G=
XM_011538981.1:c.*6G= (MTRFR)	XP_011537283.1:n.*6G=
XM_011538982.1:c.*6G= (MTRFR)	XP_011537284.1:n.*6G=
XR_945472.1:n.186+2006C=
XM_005253630.4:c.*6G= (MTRFR)	XP_005253687.1:n.*6G=
XM_011538980.3:c.*6G= (MTRFR)	XP_011537282.1:n.*6G=
XM_024449273.1:c.*6G= (MTRFR)	XP_024305041.1:n.*6G=
NM_152269.5:c.*6G= (MTRFR) MANE Select	NP_689482.1:n.*6G=