Canonical Allele Identifier: CA400850180

Gene: MAP2K6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69517530C>A , CM000679.2:g.69517530C>A	GRCh38
NC_000017.10:g.67513671C>A , CM000679.1:g.67513671C>A	GRCh37
NC_000017.9:g.65025266C>A	NCBI36
NG_029437.1:g.107834C>A
NG_029437.2:g.107834C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002758.4:c.163C>A MANE Select	NP_002749.2:p.Pro55Thr
ENST00000590474.7:c.163C>A MANE Select	ENSP00000468348.1:p.Pro55Thr
NM_001330450.1:c.-6C>A	NP_001317379.1:n.-6C>A
NM_001330450.2:c.-6C>A	NP_001317379.1:n.-6C>A
NM_002758.3:c.163C>A	NP_002749.2:p.Pro55Thr
ENST00000359094.7:c.163C>A	ENSP00000351997.3:p.Pro55Thr
ENST00000586641.5:n.437C>A
ENST00000588110.5:c.172C>A	ENSP00000464916.1:p.Pro58Thr
ENST00000589295.5:c.-6C>A	ENSP00000466143.1:n.-6C>A
ENST00000589647.5:c.-6C>A	ENSP00000467213.1:n.-6C>A
ENST00000590474.5:c.163C>A	ENSP00000468348.1:p.Pro55Thr
ENST00000591445.1:n.479C>A
ENST00000613873.4:c.-6C>A	ENSP00000477701.1:n.-6C>A
XM_005257515.1:c.-6C>A	XP_005257572.1:n.-6C>A
XM_005257516.1:c.-6C>A	XP_005257573.1:n.-6C>A
XM_005257516.2:c.-6C>A	XP_005257573.1:n.-6C>A
XM_006721975.2:c.-6C>A	XP_006722038.1:n.-6C>A
XM_006721975.3:c.-6C>A	XP_006722038.1:n.-6C>A
XM_011525025.1:c.196C>A	XP_011523327.1:p.Pro66Thr
XM_011525026.1:c.172C>A	XP_011523328.1:p.Pro58Thr
XM_011525026.2:c.172C>A	XP_011523328.1:p.Pro58Thr
XM_011525027.1:c.-6C>A	XP_011523329.1:n.-6C>A
XM_011525027.3:c.-6C>A	XP_011523329.1:n.-6C>A