Canonical Allele Identifier: CA2184658044
Gene: MAP2K5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67745287C= , CM000677.2:g.67745287C= GRCh38
NC_000015.9:g.68037625C= , CM000677.1:g.68037625C= GRCh37
NC_000015.8:g.65824679C= NCBI36
NG_029143.1:g.207605C=

Transcript Alleles

HGVS Amino-acid change
ENST00000178640.10:c.1075-2944C= MANE Select ENSP00000178640.5:n.1075-2944C=
ENST00000178640.9:c.1075-2944C= ENSP00000178640.5:n.1075-2944C=
ENST00000340972.8:c.505-2944C= ENSP00000342101.4:n.505-2944C=
ENST00000354498.9:c.967-2944C= ENSP00000346493.5:n.967-2944C=
ENST00000395476.6:c.1045-2944C= ENSP00000378859.2:n.1045-2944C=
ENST00000557869.2:c.52-3282C= ENSP00000483771.1:n.52-3282C=
ENST00000558274.1:n.186-3282C=
ENST00000558392.5:n.901-2944C=
NM_001206804.1:c.967-2944C= NP_001193733.1:n.967-2944C=
NM_002757.3:c.1045-2944C= NP_002748.1:n.1045-2944C=
NM_145160.2:c.1075-2944C= NP_660143.1:n.1075-2944C=
XM_011521784.1:c.1075-2944C= XP_011520086.1:n.1075-2944C=
XM_011521785.1:c.1075-2944C= XP_011520087.1:n.1075-2944C=
XM_011521786.1:c.1075-3282C= XP_011520088.1:n.1075-3282C=
XM_024449988.1:c.844-2944C= XP_024305756.1:n.844-2944C=
NM_145160.3:c.1075-2944C= MANE Select NP_660143.1:n.1075-2944C=
NM_001206804.2:c.967-2944C= NP_001193733.1:n.967-2944C=
NM_002757.4:c.1045-2944C= NP_002748.1:n.1045-2944C=