Canonical Allele Identifier: CA7623935

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66443262T>C , CM000677.2:g.66443262T>C	GRCh38
NC_000015.9:g.66735600T>C , CM000677.1:g.66735600T>C	GRCh37
NC_000015.8:g.64522654T>C	NCBI36
NG_008305.1:g.61390T>C , LRG_725:g.61390T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002755.4:c.439-18T>C MANE Select	NP_002746.1:n.439-18T>C
ENST00000307102.10:c.439-18T>C MANE Select	ENSP00000302486.5:n.439-18T>C
NM_002755.3:c.439-18T>C , LRG_725t1:c.439-18T>C	NP_002746.1:n.439-18T>C
ENST00000307102.9:c.439-18T>C	ENSP00000302486.4:n.439-18T>C
ENST00000425818.2:n.950-18T>C
ENST00000684779.1:c.373-18T>C	ENSP00000508681.1:n.373-18T>C
ENST00000685172.1:c.439-18T>C	ENSP00000509604.1:n.439-18T>C
ENST00000685763.1:c.292-18T>C	ENSP00000509016.1:n.292-18T>C
ENST00000686347.1:c.439-18T>C	ENSP00000509027.1:n.439-18T>C
ENST00000687191.1:n.875-1394T>C
ENST00000689951.1:c.439-18T>C	ENSP00000509308.1:n.439-18T>C
ENST00000691077.1:c.439-18T>C	ENSP00000509843.1:n.439-18T>C
ENST00000691576.1:c.439-18T>C	ENSP00000510066.1:n.439-18T>C
ENST00000691937.1:c.439-18T>C	ENSP00000508768.1:n.439-18T>C
ENST00000692487.1:c.439-18T>C	ENSP00000509534.1:n.439-18T>C
ENST00000692683.1:c.373-18T>C	ENSP00000508437.1:n.373-18T>C
ENST00000693150.1:c.373-1394T>C	ENSP00000510309.1:n.373-1394T>C
XM_011521783.1:c.373-18T>C	XP_011520085.1:n.373-18T>C
XM_011521783.3:c.373-18T>C	XP_011520085.1:n.373-18T>C
XM_017022411.2:c.439-1394T>C	XP_016877900.1:n.439-1394T>C
XM_017022412.1:c.373-1394T>C	XP_016877901.1:n.373-1394T>C