Canonical Allele Identifier: CA2499223046

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66489205G>C , CM000677.2:g.66489205G>C	GRCh38
NC_000015.9:g.66781543G>C , CM000677.1:g.66781543G>C	GRCh37
NC_000015.8:g.64568597G>C	NCBI36
NG_008305.1:g.107333G>C , LRG_725:g.107333G>C
NG_051234.1:g.13611C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002755.4:c.961-10G>C MANE Select	NP_002746.1:n.961-10G>C
ENST00000307102.10:c.961-10G>C MANE Select	ENSP00000302486.5:n.961-10G>C
NM_002755.3:c.961-10G>C , LRG_725t1:c.961-10G>C	NP_002746.1:n.961-10G>C
ENST00000307102.9:c.961-10G>C	ENSP00000302486.4:n.961-10G>C
ENST00000566326.1:c.433-10G>C	ENSP00000456438.1:n.433-10G>C
ENST00000684779.1:c.*9-10G>C	ENSP00000508681.1:n.*9-10G>C
ENST00000685172.1:c.961-10G>C	ENSP00000509604.1:n.961-10G>C
ENST00000685763.1:c.814-10G>C	ENSP00000509016.1:n.814-10G>C
ENST00000686347.1:c.634-10G>C	ENSP00000509027.1:n.634-10G>C
ENST00000687191.1:n.3231G>C
ENST00000687481.1:n.376-10G>C
ENST00000688689.1:n.716-10G>C
ENST00000689951.1:c.1012-10G>C	ENSP00000509308.1:n.1012-10G>C
ENST00000691077.1:c.*2110G>C	ENSP00000509843.1:n.*2110G>C
ENST00000691576.1:c.832-10G>C	ENSP00000510066.1:n.832-10G>C
ENST00000691937.1:c.896-10G>C	ENSP00000508768.1:n.896-10G>C
ENST00000692487.1:c.*2110G>C	ENSP00000509534.1:n.*2110G>C
ENST00000692683.1:c.895-10G>C	ENSP00000508437.1:n.895-10G>C
ENST00000693150.1:c.817-10G>C	ENSP00000510309.1:n.817-10G>C
XM_011521783.1:c.895-10G>C	XP_011520085.1:n.895-10G>C
XM_011521783.3:c.895-10G>C	XP_011520085.1:n.895-10G>C
XM_017022411.2:c.883-10G>C	XP_016877900.1:n.883-10G>C
XM_017022412.1:c.817-10G>C	XP_016877901.1:n.817-10G>C
XM_017022413.1:c.433-10G>C	XP_016877902.1:n.433-10G>C