Canonical Allele Identifier: CA2582144734

Gene: MAP2K2

Linked Data

• gnomAD v3: 19-4099545-T-TA
• gnomAD v4: 19-4099545-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099546dup , CM000681.2:g.4099546dup	GRCh38
NC_000019.9:g.4099544dup , CM000681.1:g.4099544dup	GRCh37
NC_000019.8:g.4050544dup	NCBI36
NG_007996.1:g.29583dup , LRG_750:g.29583dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-132dup
ENST00000687128.1:n.1145-132dup
ENST00000688002.1:n.868dup
ENST00000689792.1:n.646-168dup
ENST00000262948.10:c.706-132dup MANE Select	ENSP00000262948.4:n.706-132dup
ENST00000262948.9:c.706-132dup	ENSP00000262948.3:n.706-132dup
ENST00000394867.8:c.415-132dup	ENSP00000378336.1:n.415-132dup
ENST00000593364.5:n.653-132dup
ENST00000595715.1:n.389dup
ENST00000597263.5:n.169+1473dup
ENST00000599021.1:c.29+1473dup
ENST00000600584.5:n.1134dup
ENST00000601786.5:n.1007-132dup
ENST00000602167.5:n.426-132dup
NM_030662.3:c.706-132dup , LRG_750t1:c.706-132dup	NP_109587.1:n.706-132dup
XM_006722799.2:c.705+1473dup	XP_006722862.1:n.705+1473dup
XM_011528133.1:c.136-132dup	XP_011526435.1:n.136-132dup
XM_017026989.1:c.706-132dup	XP_016882478.1:n.706-132dup
XM_017026990.1:c.705+1473dup	XP_016882479.1:n.705+1473dup
XM_017026991.1:c.*184dup	XP_016882480.1:n.*184dup
NM_030662.4:c.706-132dup MANE Select	NP_109587.1:n.706-132dup