Canonical Allele Identifier: CA7624067

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66489215C>T , CM000677.2:g.66489215C>T	GRCh38
NC_000015.9:g.66781553C>T , CM000677.1:g.66781553C>T	GRCh37
NC_000015.8:g.64568607C>T	NCBI36
NG_008305.1:g.107343C>T , LRG_725:g.107343C>T
NG_051234.1:g.13601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*9C>T	ENSP00000508681.1:n.*9C>T
ENST00000685172.1:c.961C>T	ENSP00000509604.1:p.Pro321Ser
ENST00000685763.1:c.814C>T	ENSP00000509016.1:p.Pro272Ser
ENST00000686347.1:c.634C>T	ENSP00000509027.1:p.Pro212Ser
ENST00000687191.1:n.3241C>T
ENST00000687481.1:n.376C>T
ENST00000688689.1:n.716C>T
ENST00000689951.1:c.1012C>T	ENSP00000509308.1:p.Pro338Ser
ENST00000691077.1:c.*2120C>T	ENSP00000509843.1:n.*2120C>T
ENST00000691576.1:c.832C>T	ENSP00000510066.1:p.Pro278Ser
ENST00000691937.1:c.896C>T	ENSP00000508768.1:p.Ser299Phe
ENST00000692487.1:c.*2120C>T	ENSP00000509534.1:n.*2120C>T
ENST00000692683.1:c.895C>T	ENSP00000508437.1:p.Pro299Ser
ENST00000693150.1:c.817C>T	ENSP00000510309.1:p.Pro273Ser
ENST00000307102.10:c.961C>T MANE Select	ENSP00000302486.5:p.Pro321Ser
ENST00000307102.9:c.961C>T	ENSP00000302486.4:p.Pro321Ser
ENST00000566326.1:c.433C>T	ENSP00000456438.1:p.Pro145Ser
NM_002755.3:c.961C>T , LRG_725t1:c.961C>T	NP_002746.1:p.Pro321Ser
XM_011521783.1:c.895C>T	XP_011520085.1:p.Pro299Ser
XM_011521783.3:c.895C>T	XP_011520085.1:p.Pro299Ser
XM_017022411.2:c.883C>T	XP_016877900.1:p.Pro295Ser
XM_017022412.1:c.817C>T	XP_016877901.1:p.Pro273Ser
XM_017022413.1:c.433C>T	XP_016877902.1:p.Pro145Ser
NM_002755.4:c.961C>T MANE Select	NP_002746.1:p.Pro321Ser