Canonical Allele Identifier: CA400850206

Gene: MAP2K6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69517537T>C , CM000679.2:g.69517537T>C	GRCh38
NC_000017.10:g.67513678T>C , CM000679.1:g.67513678T>C	GRCh37
NC_000017.9:g.65025273T>C	NCBI36
NG_029437.1:g.107841T>C
NG_029437.2:g.107841T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002758.4:c.170T>C MANE Select	NP_002749.2:p.Met57Thr
ENST00000590474.7:c.170T>C MANE Select	ENSP00000468348.1:p.Met57Thr
NM_001330450.1:c.2T>C	NP_001317379.1:p.Met1Thr
NM_001330450.2:c.2T>C	NP_001317379.1:p.Met1Thr
NM_002758.3:c.170T>C	NP_002749.2:p.Met57Thr
ENST00000359094.7:c.170T>C	ENSP00000351997.3:p.Met57Thr
ENST00000586641.5:n.444T>C
ENST00000588110.5:c.179T>C	ENSP00000464916.1:p.Met60Thr
ENST00000589295.5:c.2T>C	ENSP00000466143.1:p.Met1Thr
ENST00000589647.5:c.2T>C	ENSP00000467213.1:p.Met1Thr
ENST00000590474.5:c.170T>C	ENSP00000468348.1:p.Met57Thr
ENST00000591445.1:n.486T>C
ENST00000613873.4:c.2T>C	ENSP00000477701.1:p.Met1Thr
XM_005257515.1:c.2T>C	XP_005257572.1:p.Met1Thr
XM_005257516.1:c.2T>C	XP_005257573.1:p.Met1Thr
XM_005257516.2:c.2T>C	XP_005257573.1:p.Met1Thr
XM_006721975.2:c.2T>C	XP_006722038.1:p.Met1Thr
XM_006721975.3:c.2T>C	XP_006722038.1:p.Met1Thr
XM_011525025.1:c.203T>C	XP_011523327.1:p.Met68Thr
XM_011525026.1:c.179T>C	XP_011523328.1:p.Met60Thr
XM_011525026.2:c.179T>C	XP_011523328.1:p.Met60Thr
XM_011525027.1:c.2T>C	XP_011523329.1:p.Met1Thr
XM_011525027.3:c.2T>C	XP_011523329.1:p.Met1Thr