Canonical Allele Identifier: CA2184071645

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66434897_66434898delinsTC , CM000677.2:g.66434897_66434898delinsTC	GRCh38
NC_000015.9:g.66727235_66727236delinsTC , CM000677.1:g.66727235_66727236delinsTC	GRCh37
NC_000015.8:g.64514289_64514290delinsTC	NCBI36
NG_008305.1:g.53025_53026delinsTC , LRG_725:g.53025_53026delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000684779.1:c.15-130_15-129delinsTC	ENSP00000508681.1:n.15-130_15-129delinsTC
ENST00000685172.1:c.81-130_81-129delinsTC	ENSP00000509604.1:n.81-130_81-129delinsTC
ENST00000685763.1:c.81-130_81-129delinsTC	ENSP00000509016.1:n.81-130_81-129delinsTC
ENST00000686347.1:c.81-130_81-129delinsTC	ENSP00000509027.1:n.81-130_81-129delinsTC
ENST00000687191.1:n.517-130_517-129delinsTC
ENST00000689951.1:c.81-130_81-129delinsTC	ENSP00000509308.1:n.81-130_81-129delinsTC
ENST00000691077.1:c.81-130_81-129delinsTC	ENSP00000509843.1:n.81-130_81-129delinsTC
ENST00000691576.1:c.81-130_81-129delinsTC	ENSP00000510066.1:n.81-130_81-129delinsTC
ENST00000691937.1:c.81-130_81-129delinsTC	ENSP00000508768.1:n.81-130_81-129delinsTC
ENST00000692487.1:c.81-130_81-129delinsTC	ENSP00000509534.1:n.81-130_81-129delinsTC
ENST00000692683.1:c.15-130_15-129delinsTC	ENSP00000508437.1:n.15-130_15-129delinsTC
ENST00000693150.1:c.15-130_15-129delinsTC	ENSP00000510309.1:n.15-130_15-129delinsTC
ENST00000307102.10:c.81-130_81-129delinsTC MANE Select	ENSP00000302486.5:n.81-130_81-129delinsTC
ENST00000307102.9:c.81-130_81-129delinsTC	ENSP00000302486.4:n.81-130_81-129delinsTC
ENST00000425818.2:n.592-130_592-129delinsTC
NM_002755.3:c.81-130_81-129delinsTC , LRG_725t1:c.81-130_81-129delinsTC	NP_002746.1:n.81-130_81-129delinsTC
XM_011521783.1:c.15-130_15-129delinsTC	XP_011520085.1:n.15-130_15-129delinsTC
XM_011521783.3:c.15-130_15-129delinsTC	XP_011520085.1:n.15-130_15-129delinsTC
XM_017022411.2:c.81-130_81-129delinsTC	XP_016877900.1:n.81-130_81-129delinsTC
XM_017022412.1:c.15-130_15-129delinsTC	XP_016877901.1:n.15-130_15-129delinsTC
NM_002755.4:c.81-130_81-129delinsTC MANE Select	NP_002746.1:n.81-130_81-129delinsTC