Canonical Allele Identifier: CA2272697871

Gene: MAP2K6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69517534T= , CM000679.2:g.69517534T=	GRCh38
NC_000017.10:g.67513675T= , CM000679.1:g.67513675T=	GRCh37
NC_000017.9:g.65025270T=	NCBI36
NG_029437.1:g.107838T=
NG_029437.2:g.107838T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002758.4:c.167T= MANE Select	NP_002749.2:p.Ile56=
ENST00000590474.7:c.167T= MANE Select	ENSP00000468348.1:p.Ile56=
NM_001330450.1:c.-2T=	NP_001317379.1:n.-2T=
NM_001330450.2:c.-2T=	NP_001317379.1:n.-2T=
NM_002758.3:c.167T=	NP_002749.2:p.Ile56=
ENST00000359094.7:c.167T=	ENSP00000351997.3:p.Ile56=
ENST00000586641.5:n.441T=
ENST00000588110.5:c.176T=	ENSP00000464916.1:p.Ile59=
ENST00000589295.5:c.-2T=	ENSP00000466143.1:n.-2T=
ENST00000589647.5:c.-2T=	ENSP00000467213.1:n.-2T=
ENST00000590474.5:c.167T=	ENSP00000468348.1:p.Ile56=
ENST00000591445.1:n.483T=
ENST00000613873.4:c.-2T=	ENSP00000477701.1:n.-2T=
XM_005257515.1:c.-2T=	XP_005257572.1:n.-2T=
XM_005257516.1:c.-2T=	XP_005257573.1:n.-2T=
XM_005257516.2:c.-2T=	XP_005257573.1:n.-2T=
XM_006721975.2:c.-2T=	XP_006722038.1:n.-2T=
XM_006721975.3:c.-2T=	XP_006722038.1:n.-2T=
XM_011525025.1:c.200T=	XP_011523327.1:p.Ile67=
XM_011525026.1:c.176T=	XP_011523328.1:p.Ile59=
XM_011525026.2:c.176T=	XP_011523328.1:p.Ile59=
XM_011525027.1:c.-2T=	XP_011523329.1:n.-2T=
XM_011525027.3:c.-2T=	XP_011523329.1:n.-2T=