Canonical Allele Identifier: CA2582144709

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145042215
• gnomAD v3: 19-4094671-AG-A
• gnomAD v4: 19-4094671-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094674del , CM000681.2:g.4094674del	GRCh38
NC_000019.9:g.4094672del , CM000681.1:g.4094672del	GRCh37
NC_000019.8:g.4045672del	NCBI36
NG_007996.1:g.34457del , LRG_750:g.34457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-174del
ENST00000688002.1:n.3198-174del
ENST00000688751.1:n.183-174del
ENST00000689792.1:n.951-174del
ENST00000262948.10:c.1047-174del MANE Select	ENSP00000262948.4:n.1047-174del
ENST00000262948.9:c.1047-174del	ENSP00000262948.3:n.1047-174del
ENST00000394867.8:c.756-174del	ENSP00000378336.1:n.756-174del
ENST00000597263.5:n.232-174del
ENST00000599021.1:c.157-174del
ENST00000600584.5:n.2322del
ENST00000601786.5:n.1348-174del
NM_030662.3:c.1047-174del , LRG_750t1:c.1047-174del	NP_109587.1:n.1047-174del
XM_006722799.2:c.768-174del	XP_006722862.1:n.768-174del
XM_011528133.1:c.477-174del	XP_011526435.1:n.477-174del
XM_017026989.1:c.1421del	XP_016882478.1:p.Pro474LeufsTer?
XM_017026990.1:c.1142del	XP_016882479.1:p.Pro381LeufsTer?
NM_030662.4:c.1047-174del MANE Select	NP_109587.1:n.1047-174del