Canonical Allele Identifier: CA2585249256

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4110471-G-GGAGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110472_4110477dup , CM000681.2:g.4110472_4110477dup	GRCh38
NC_000019.9:g.4110470_4110475dup , CM000681.1:g.4110470_4110475dup	GRCh37
NC_000019.8:g.4061470_4061475dup	NCBI36
NG_007996.1:g.18652_18657dup , LRG_750:g.18652_18657dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.889+32_889+37dup
ENST00000687128.1:n.889+32_889+37dup
ENST00000262948.10:c.450+32_450+37dup MANE Select	ENSP00000262948.4:n.450+32_450+37dup
ENST00000262948.9:c.450+32_450+37dup	ENSP00000262948.3:n.450+32_450+37dup
ENST00000394867.8:c.159+32_159+37dup	ENSP00000378336.1:n.159+32_159+37dup
ENST00000599345.1:n.647+32_647+37dup
NM_030662.3:c.450+32_450+37dup , LRG_750t1:c.450+32_450+37dup	NP_109587.1:n.450+32_450+37dup
XM_006722799.2:c.450+32_450+37dup	XP_006722862.1:n.450+32_450+37dup
XM_017026989.1:c.450+32_450+37dup	XP_016882478.1:n.450+32_450+37dup
XM_017026990.1:c.450+32_450+37dup	XP_016882479.1:n.450+32_450+37dup
XM_017026991.1:c.450+32_450+37dup	XP_016882480.1:n.450+32_450+37dup
NM_030662.4:c.450+32_450+37dup MANE Select	NP_109587.1:n.450+32_450+37dup