Canonical Allele Identifier: CA400850199

Gene: MAP2K6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69517535A>G , CM000679.2:g.69517535A>G	GRCh38
NC_000017.10:g.67513676A>G , CM000679.1:g.67513676A>G	GRCh37
NC_000017.9:g.65025271A>G	NCBI36
NG_029437.1:g.107839A>G
NG_029437.2:g.107839A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002758.4:c.168A>G MANE Select	NP_002749.2:p.Ile56Met
ENST00000590474.7:c.168A>G MANE Select	ENSP00000468348.1:p.Ile56Met
NM_001330450.1:c.-1A>G	NP_001317379.1:n.-1A>G
NM_001330450.2:c.-1A>G	NP_001317379.1:n.-1A>G
NM_002758.3:c.168A>G	NP_002749.2:p.Ile56Met
ENST00000359094.7:c.168A>G	ENSP00000351997.3:p.Ile56Met
ENST00000586641.5:n.442A>G
ENST00000588110.5:c.177A>G	ENSP00000464916.1:p.Ile59Met
ENST00000589295.5:c.-1A>G	ENSP00000466143.1:n.-1A>G
ENST00000589647.5:c.-1A>G	ENSP00000467213.1:n.-1A>G
ENST00000590474.5:c.168A>G	ENSP00000468348.1:p.Ile56Met
ENST00000591445.1:n.484A>G
ENST00000613873.4:c.-1A>G	ENSP00000477701.1:n.-1A>G
XM_005257515.1:c.-1A>G	XP_005257572.1:n.-1A>G
XM_005257516.1:c.-1A>G	XP_005257573.1:n.-1A>G
XM_005257516.2:c.-1A>G	XP_005257573.1:n.-1A>G
XM_006721975.2:c.-1A>G	XP_006722038.1:n.-1A>G
XM_006721975.3:c.-1A>G	XP_006722038.1:n.-1A>G
XM_011525025.1:c.201A>G	XP_011523327.1:p.Ile67Met
XM_011525026.1:c.177A>G	XP_011523328.1:p.Ile59Met
XM_011525026.2:c.177A>G	XP_011523328.1:p.Ile59Met
XM_011525027.1:c.-1A>G	XP_011523329.1:n.-1A>G
XM_011525027.3:c.-1A>G	XP_011523329.1:n.-1A>G