Canonical Allele Identifier: CA2184660218

Gene: MAP2K5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67750719C>T , CM000677.2:g.67750719C>T	GRCh38
NC_000015.9:g.68043057C>T , CM000677.1:g.68043057C>T	GRCh37
NC_000015.8:g.65830111C>T	NCBI36
NG_029143.1:g.213037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178640.10:c.1134+2118C>T MANE Select	ENSP00000178640.5:n.1134+2118C>T
ENST00000178640.9:c.1134+2118C>T	ENSP00000178640.5:n.1134+2118C>T
ENST00000340972.8:c.564+2118C>T	ENSP00000342101.4:n.564+2118C>T
ENST00000354498.9:c.1026+2118C>T	ENSP00000346493.5:n.1026+2118C>T
ENST00000395476.6:c.1104+2118C>T	ENSP00000378859.2:n.1104+2118C>T
ENST00000557869.2:c.84+2118C>T	ENSP00000483771.1:n.84+2118C>T
ENST00000558021.1:n.234+2118C>T
ENST00000558274.1:n.218+2118C>T
ENST00000558392.5:n.960+2118C>T
NM_001206804.1:c.1026+2118C>T	NP_001193733.1:n.1026+2118C>T
NM_002757.3:c.1104+2118C>T	NP_002748.1:n.1104+2118C>T
NM_145160.2:c.1134+2118C>T	NP_660143.1:n.1134+2118C>T
XM_011521784.1:c.1134+2118C>T	XP_011520086.1:n.1134+2118C>T
XM_011521785.1:c.1134+2118C>T	XP_011520087.1:n.1134+2118C>T
XM_011521786.1:c.1107+2118C>T	XP_011520088.1:n.1107+2118C>T
XM_024449988.1:c.903+2118C>T	XP_024305756.1:n.903+2118C>T
NM_145160.3:c.1134+2118C>T MANE Select	NP_660143.1:n.1134+2118C>T
NM_001206804.2:c.1026+2118C>T	NP_001193733.1:n.1026+2118C>T
NM_002757.4:c.1104+2118C>T	NP_002748.1:n.1104+2118C>T