Canonical Allele Identifier: CA2184658045
Gene: MAP2K5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67745288G= , CM000677.2:g.67745288G= GRCh38
NC_000015.9:g.68037626G= , CM000677.1:g.68037626G= GRCh37
NC_000015.8:g.65824680G= NCBI36
NG_029143.1:g.207606G=

Transcript Alleles

HGVS Amino-acid change
ENST00000178640.10:c.1075-2943G= MANE Select ENSP00000178640.5:n.1075-2943G=
ENST00000178640.9:c.1075-2943G= ENSP00000178640.5:n.1075-2943G=
ENST00000340972.8:c.505-2943G= ENSP00000342101.4:n.505-2943G=
ENST00000354498.9:c.967-2943G= ENSP00000346493.5:n.967-2943G=
ENST00000395476.6:c.1045-2943G= ENSP00000378859.2:n.1045-2943G=
ENST00000557869.2:c.52-3281G= ENSP00000483771.1:n.52-3281G=
ENST00000558274.1:n.186-3281G=
ENST00000558392.5:n.901-2943G=
NM_001206804.1:c.967-2943G= NP_001193733.1:n.967-2943G=
NM_002757.3:c.1045-2943G= NP_002748.1:n.1045-2943G=
NM_145160.2:c.1075-2943G= NP_660143.1:n.1075-2943G=
XM_011521784.1:c.1075-2943G= XP_011520086.1:n.1075-2943G=
XM_011521785.1:c.1075-2943G= XP_011520087.1:n.1075-2943G=
XM_011521786.1:c.1075-3281G= XP_011520088.1:n.1075-3281G=
XM_024449988.1:c.844-2943G= XP_024305756.1:n.844-2943G=
NM_145160.3:c.1075-2943G= MANE Select NP_660143.1:n.1075-2943G=
NM_001206804.2:c.967-2943G= NP_001193733.1:n.967-2943G=
NM_002757.4:c.1045-2943G= NP_002748.1:n.1045-2943G=