Canonical Allele Identifier: CA2184677713

Gene: MAP2K5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67807105C= , CM000677.2:g.67807105C=	GRCh38
NC_000015.9:g.68099443C= , CM000677.1:g.68099443C=	GRCh37
NC_000015.8:g.65886497C=	NCBI36
NG_029143.1:g.269423C=

Transcript Alleles

HGVS	Amino-acid Change
NM_145160.3:c.*355C= MANE Select	NP_660143.1:n.*355C=
ENST00000178640.10:c.*355C= MANE Select	ENSP00000178640.5:n.*355C=
NM_001206804.1:c.*355C=	NP_001193733.1:n.*355C=
NM_001206804.2:c.*355C=	NP_001193733.1:n.*355C=
NM_002757.3:c.*355C=	NP_002748.1:n.*355C=
NM_002757.4:c.*355C=	NP_002748.1:n.*355C=
NM_145160.2:c.*355C=	NP_660143.1:n.*355C=
ENST00000178640.9:c.*355C=	ENSP00000178640.5:n.*355C=
ENST00000340972.8:c.*355C=	ENSP00000342101.4:n.*355C=
ENST00000354498.9:c.*355C=	ENSP00000346493.5:n.*355C=
ENST00000395476.6:c.*355C=	ENSP00000378859.2:n.*355C=
XM_011521784.1:c.*355C=	XP_011520086.1:n.*355C=
XM_011521786.1:c.*355C=	XP_011520088.1:n.*355C=
XM_024449988.1:c.*355C=	XP_024305756.1:n.*355C=