Canonical Allele Identifier: CA2584877126

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094665-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094666_4094667del , CM000681.2:g.4094666_4094667del	GRCh38
NC_000019.9:g.4094664_4094665del , CM000681.1:g.4094664_4094665del	GRCh37
NC_000019.8:g.4045664_4045665del	NCBI36
NG_007996.1:g.34462_34463del , LRG_750:g.34462_34463del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-169_1486-168del
ENST00000688002.1:n.3198-169_3198-168del
ENST00000688751.1:n.183-169_183-168del
ENST00000689792.1:n.951-169_951-168del
ENST00000262948.10:c.1047-169_1047-168del MANE Select	ENSP00000262948.4:n.1047-169_1047-168del
ENST00000262948.9:c.1047-169_1047-168del	ENSP00000262948.3:n.1047-169_1047-168del
ENST00000394867.8:c.756-169_756-168del	ENSP00000378336.1:n.756-169_756-168del
ENST00000597263.5:n.232-169_232-168del
ENST00000599021.1:c.157-169_157-168del
ENST00000600584.5:n.2327_2328del
ENST00000601786.5:n.1348-169_1348-168del
NM_030662.3:c.1047-169_1047-168del , LRG_750t1:c.1047-169_1047-168del	NP_109587.1:n.1047-169_1047-168del
XM_006722799.2:c.768-169_768-168del	XP_006722862.1:n.768-169_768-168del
XM_011528133.1:c.477-169_477-168del	XP_011526435.1:n.477-169_477-168del
XM_017026989.1:c.1426_1427del	XP_016882478.1:p.Pro476SerfsTer?
XM_017026990.1:c.1147_1148del	XP_016882479.1:p.Pro383SerfsTer?
NM_030662.4:c.1047-169_1047-168del MANE Select	NP_109587.1:n.1047-169_1047-168del