Canonical Allele Identifier: CA2184657979

Gene: MAP2K5

Linked Data

• dbSNP Id: rs2089576316

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67745142T>C , CM000677.2:g.67745142T>C	GRCh38
NC_000015.9:g.68037480T>C , CM000677.1:g.68037480T>C	GRCh37
NC_000015.8:g.65824534T>C	NCBI36
NG_029143.1:g.207460T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000178640.10:c.1075-3089T>C MANE Select	ENSP00000178640.5:n.1075-3089T>C
ENST00000178640.9:c.1075-3089T>C	ENSP00000178640.5:n.1075-3089T>C
ENST00000340972.8:c.505-3089T>C	ENSP00000342101.4:n.505-3089T>C
ENST00000354498.9:c.967-3089T>C	ENSP00000346493.5:n.967-3089T>C
ENST00000395476.6:c.1045-3089T>C	ENSP00000378859.2:n.1045-3089T>C
ENST00000557869.2:c.52-3427T>C	ENSP00000483771.1:n.52-3427T>C
ENST00000558274.1:n.186-3427T>C
ENST00000558392.5:n.901-3089T>C
NM_001206804.1:c.967-3089T>C	NP_001193733.1:n.967-3089T>C
NM_002757.3:c.1045-3089T>C	NP_002748.1:n.1045-3089T>C
NM_145160.2:c.1075-3089T>C	NP_660143.1:n.1075-3089T>C
XM_011521784.1:c.1075-3089T>C	XP_011520086.1:n.1075-3089T>C
XM_011521785.1:c.1075-3089T>C	XP_011520087.1:n.1075-3089T>C
XM_011521786.1:c.1075-3427T>C	XP_011520088.1:n.1075-3427T>C
XM_024449988.1:c.844-3089T>C	XP_024305756.1:n.844-3089T>C
NM_145160.3:c.1075-3089T>C MANE Select	NP_660143.1:n.1075-3089T>C
NM_001206804.2:c.967-3089T>C	NP_001193733.1:n.967-3089T>C
NM_002757.4:c.1045-3089T>C	NP_002748.1:n.1045-3089T>C