Canonical Allele Identifier: CA992819107

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1461669930
• gnomAD v3: 19-4094709-AC-A
• gnomAD v4: 19-4094709-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094715del , CM000681.2:g.4094715del	GRCh38
NC_000019.9:g.4094713del , CM000681.1:g.4094713del	GRCh37
NC_000019.8:g.4045713del	NCBI36
NG_007996.1:g.34419del , LRG_750:g.34419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-212del
ENST00000688002.1:n.3198-212del
ENST00000688751.1:n.183-212del
ENST00000689792.1:n.951-212del
ENST00000262948.10:c.1047-212del MANE Select	ENSP00000262948.4:n.1047-212del
ENST00000262948.9:c.1047-212del	ENSP00000262948.3:n.1047-212del
ENST00000394867.8:c.756-212del	ENSP00000378336.1:n.756-212del
ENST00000597263.5:n.232-212del
ENST00000599021.1:c.157-212del
ENST00000600584.5:n.2284del
ENST00000601786.5:n.1348-212del
NM_030662.3:c.1047-212del , LRG_750t1:c.1047-212del	NP_109587.1:n.1047-212del
XM_006722799.2:c.768-212del	XP_006722862.1:n.768-212del
XM_011528133.1:c.477-212del	XP_011526435.1:n.477-212del
XM_017026989.1:c.1383del	XP_016882478.1:p.Cys462ValfsTer?
XM_017026990.1:c.1104del	XP_016882479.1:p.Cys369ValfsTer?
NM_030662.4:c.1047-212del MANE Select	NP_109587.1:n.1047-212del