Canonical Allele Identifier: CA715112856

Gene: MAP2K5

Linked Data

• dbSNP Id: rs1246546914
• MyVariant Identifiers: chr15:g.68037615del (hg19) ; chr15:g.67745277del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67745278del , CM000677.2:g.67745278del	GRCh38
NC_000015.9:g.68037616del , CM000677.1:g.68037616del	GRCh37
NC_000015.8:g.65824670del	NCBI36
NG_029143.1:g.207596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178640.10:c.1075-2953del MANE Select	ENSP00000178640.5:n.1075-2953del
ENST00000178640.9:c.1075-2953del	ENSP00000178640.5:n.1075-2953del
ENST00000340972.8:c.505-2953del	ENSP00000342101.4:n.505-2953del
ENST00000354498.9:c.967-2953del	ENSP00000346493.5:n.967-2953del
ENST00000395476.6:c.1045-2953del	ENSP00000378859.2:n.1045-2953del
ENST00000557869.2:c.52-3291del	ENSP00000483771.1:n.52-3291del
ENST00000558274.1:n.186-3291del
ENST00000558392.5:n.901-2953del
NM_001206804.1:c.967-2953del	NP_001193733.1:n.967-2953del
NM_002757.3:c.1045-2953del	NP_002748.1:n.1045-2953del
NM_145160.2:c.1075-2953del	NP_660143.1:n.1075-2953del
XM_011521784.1:c.1075-2953del	XP_011520086.1:n.1075-2953del
XM_011521785.1:c.1075-2953del	XP_011520087.1:n.1075-2953del
XM_011521786.1:c.1075-3291del	XP_011520088.1:n.1075-3291del
XM_024449988.1:c.844-2953del	XP_024305756.1:n.844-2953del
NM_145160.3:c.1075-2953del MANE Select	NP_660143.1:n.1075-2953del
NM_001206804.2:c.967-2953del	NP_001193733.1:n.967-2953del
NM_002757.4:c.1045-2953del	NP_002748.1:n.1045-2953del