Canonical Allele Identifier: CA400850204

Gene: MAP2K6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69517536A>G , CM000679.2:g.69517536A>G	GRCh38
NC_000017.10:g.67513677A>G , CM000679.1:g.67513677A>G	GRCh37
NC_000017.9:g.65025272A>G	NCBI36
NG_029437.1:g.107840A>G
NG_029437.2:g.107840A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002758.4:c.169A>G MANE Select	NP_002749.2:p.Met57Val
ENST00000590474.7:c.169A>G MANE Select	ENSP00000468348.1:p.Met57Val
NM_001330450.1:c.1A>G	NP_001317379.1:p.Met1Val
NM_001330450.2:c.1A>G	NP_001317379.1:p.Met1Val
NM_002758.3:c.169A>G	NP_002749.2:p.Met57Val
ENST00000359094.7:c.169A>G	ENSP00000351997.3:p.Met57Val
ENST00000586641.5:n.443A>G
ENST00000588110.5:c.178A>G	ENSP00000464916.1:p.Met60Val
ENST00000589295.5:c.1A>G	ENSP00000466143.1:p.Met1Val
ENST00000589647.5:c.1A>G	ENSP00000467213.1:p.Met1Val
ENST00000590474.5:c.169A>G	ENSP00000468348.1:p.Met57Val
ENST00000591445.1:n.485A>G
ENST00000613873.4:c.1A>G	ENSP00000477701.1:p.Met1Val
XM_005257515.1:c.1A>G	XP_005257572.1:p.Met1Val
XM_005257516.1:c.1A>G	XP_005257573.1:p.Met1Val
XM_005257516.2:c.1A>G	XP_005257573.1:p.Met1Val
XM_006721975.2:c.1A>G	XP_006722038.1:p.Met1Val
XM_006721975.3:c.1A>G	XP_006722038.1:p.Met1Val
XM_011525025.1:c.202A>G	XP_011523327.1:p.Met68Val
XM_011525026.1:c.178A>G	XP_011523328.1:p.Met60Val
XM_011525026.2:c.178A>G	XP_011523328.1:p.Met60Val
XM_011525027.1:c.1A>G	XP_011523329.1:p.Met1Val
XM_011525027.3:c.1A>G	XP_011523329.1:p.Met1Val