Canonical Allele Identifier: CA2735506296

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145043798

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095518_4095519del , CM000681.2:g.4095518_4095519del	GRCh38
NC_000019.9:g.4095516_4095517del , CM000681.1:g.4095516_4095517del	GRCh37
NC_000019.8:g.4046516_4046517del	NCBI36
NG_007996.1:g.33610_33611del , LRG_750:g.33610_33611del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-70_1424-69del
ENST00000688002.1:n.3136-70_3136-69del
ENST00000688751.1:n.121-70_121-69del
ENST00000689792.1:n.889-70_889-69del
ENST00000262948.10:c.985-70_985-69del MANE Select	ENSP00000262948.4:n.985-70_985-69del
ENST00000262948.9:c.985-70_985-69del	ENSP00000262948.3:n.985-70_985-69del
ENST00000394867.8:c.694-70_694-69del	ENSP00000378336.1:n.694-70_694-69del
ENST00000595715.1:n.800-70_800-69del
ENST00000597263.5:n.170-70_170-69del
ENST00000599021.1:c.95-70_95-69del
ENST00000600584.5:n.1545-70_1545-69del
ENST00000601786.5:n.1286-70_1286-69del
NM_030662.3:c.985-70_985-69del , LRG_750t1:c.985-70_985-69del	NP_109587.1:n.985-70_985-69del
XM_006722799.2:c.706-70_706-69del	XP_006722862.1:n.706-70_706-69del
XM_011528133.1:c.415-70_415-69del	XP_011526435.1:n.415-70_415-69del
XM_017026989.1:c.985-70_985-69del	XP_016882478.1:n.985-70_985-69del
XM_017026990.1:c.706-70_706-69del	XP_016882479.1:n.706-70_706-69del
NM_030662.4:c.985-70_985-69del MANE Select	NP_109587.1:n.985-70_985-69del