Canonical Allele Identifier: CA14084717
Gene: MAP2K5 HGNC NCBI

Linked Data

dbSNP Id: rs1026732

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67802747G>A , CM000677.2:g.67802747G>A GRCh38
NC_000015.9:g.68095085G>A , CM000677.1:g.68095085G>A GRCh37
NC_000015.8:g.65882139G>A NCBI36
NG_029143.1:g.265065G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000178640.10:c.1243-3899G>A MANE Select ENSP00000178640.5:n.1243-3899G>A
ENST00000178640.9:c.1243-3899G>A ENSP00000178640.5:n.1243-3899G>A
ENST00000340972.8:c.673-3899G>A ENSP00000342101.4:n.673-3899G>A
ENST00000354498.9:c.1135-3899G>A ENSP00000346493.5:n.1135-3899G>A
ENST00000395476.6:c.1213-3899G>A ENSP00000378859.2:n.1213-3899G>A
ENST00000558274.1:n.327-3899G>A
ENST00000558392.5:n.1069-3899G>A
NM_001206804.1:c.1135-3899G>A NP_001193733.1:n.1135-3899G>A
NM_002757.3:c.1213-3899G>A NP_002748.1:n.1213-3899G>A
NM_145160.2:c.1243-3899G>A NP_660143.1:n.1243-3899G>A
XM_011521784.1:c.1288-3899G>A XP_011520086.1:n.1288-3899G>A
XM_011521786.1:c.1216-3899G>A XP_011520088.1:n.1216-3899G>A
XM_024449988.1:c.1012-3899G>A XP_024305756.1:n.1012-3899G>A
NM_145160.3:c.1243-3899G>A MANE Select NP_660143.1:n.1243-3899G>A
NM_001206804.2:c.1135-3899G>A NP_001193733.1:n.1135-3899G>A
NM_002757.4:c.1213-3899G>A NP_002748.1:n.1213-3899G>A