Canonical Allele Identifier: CA2584877019

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094574-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094577del , CM000681.2:g.4094577del	GRCh38
NC_000019.9:g.4094575del , CM000681.1:g.4094575del	GRCh37
NC_000019.8:g.4045575del	NCBI36
NG_007996.1:g.34554del , LRG_750:g.34554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-77del
ENST00000688002.1:n.3198-77del
ENST00000688751.1:n.183-77del
ENST00000689792.1:n.951-77del
ENST00000262948.10:c.1047-77del MANE Select	ENSP00000262948.4:n.1047-77del
ENST00000262948.9:c.1047-77del	ENSP00000262948.3:n.1047-77del
ENST00000394867.8:c.756-77del	ENSP00000378336.1:n.756-77del
ENST00000597263.5:n.232-77del
ENST00000599021.1:c.157-77del
ENST00000600584.5:n.2419del
ENST00000601786.5:n.1348-77del
NM_030662.3:c.1047-77del , LRG_750t1:c.1047-77del	NP_109587.1:n.1047-77del
XM_006722799.2:c.768-77del	XP_006722862.1:n.768-77del
XM_011528133.1:c.477-77del	XP_011526435.1:n.477-77del
XM_017026989.1:c.1518del	XP_016882478.1:p.Cys507AlafsTer?
XM_017026990.1:c.1239del	XP_016882479.1:p.Cys414AlafsTer?
NM_030662.4:c.1047-77del MANE Select	NP_109587.1:n.1047-77del