Canonical Allele Identifier: CA2184658033

Gene: MAP2K5

Linked Data

• dbSNP Id: rs2089579576

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67745261_67745263dup , CM000677.2:g.67745261_67745263dup	GRCh38
NC_000015.9:g.68037599_68037601dup , CM000677.1:g.68037599_68037601dup	GRCh37
NC_000015.8:g.65824653_65824655dup	NCBI36
NG_029143.1:g.207579_207581dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178640.10:c.1075-2970_1075-2968dup MANE Select	ENSP00000178640.5:n.1075-2970_1075-2968dup
ENST00000178640.9:c.1075-2970_1075-2968dup	ENSP00000178640.5:n.1075-2970_1075-2968dup
ENST00000340972.8:c.505-2970_505-2968dup	ENSP00000342101.4:n.505-2970_505-2968dup
ENST00000354498.9:c.967-2970_967-2968dup	ENSP00000346493.5:n.967-2970_967-2968dup
ENST00000395476.6:c.1045-2970_1045-2968dup	ENSP00000378859.2:n.1045-2970_1045-2968dup
ENST00000557869.2:c.52-3308_52-3306dup	ENSP00000483771.1:n.52-3308_52-3306dup
ENST00000558274.1:n.186-3308_186-3306dup
ENST00000558392.5:n.901-2970_901-2968dup
NM_001206804.1:c.967-2970_967-2968dup	NP_001193733.1:n.967-2970_967-2968dup
NM_002757.3:c.1045-2970_1045-2968dup	NP_002748.1:n.1045-2970_1045-2968dup
NM_145160.2:c.1075-2970_1075-2968dup	NP_660143.1:n.1075-2970_1075-2968dup
XM_011521784.1:c.1075-2970_1075-2968dup	XP_011520086.1:n.1075-2970_1075-2968dup
XM_011521785.1:c.1075-2970_1075-2968dup	XP_011520087.1:n.1075-2970_1075-2968dup
XM_011521786.1:c.1075-3308_1075-3306dup	XP_011520088.1:n.1075-3308_1075-3306dup
XM_024449988.1:c.844-2970_844-2968dup	XP_024305756.1:n.844-2970_844-2968dup
NM_145160.3:c.1075-2970_1075-2968dup MANE Select	NP_660143.1:n.1075-2970_1075-2968dup
NM_001206804.2:c.967-2970_967-2968dup	NP_001193733.1:n.967-2970_967-2968dup
NM_002757.4:c.1045-2970_1045-2968dup	NP_002748.1:n.1045-2970_1045-2968dup