Canonical Allele Identifier: CA2584877115

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094655-CTCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094656_4094659del , CM000681.2:g.4094656_4094659del	GRCh38
NC_000019.9:g.4094654_4094657del , CM000681.1:g.4094654_4094657del	GRCh37
NC_000019.8:g.4045654_4045657del	NCBI36
NG_007996.1:g.34470_34473del , LRG_750:g.34470_34473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-161_1486-158del
ENST00000688002.1:n.3198-161_3198-158del
ENST00000688751.1:n.183-161_183-158del
ENST00000689792.1:n.951-161_951-158del
ENST00000262948.10:c.1047-161_1047-158del MANE Select	ENSP00000262948.4:n.1047-161_1047-158del
ENST00000262948.9:c.1047-161_1047-158del	ENSP00000262948.3:n.1047-161_1047-158del
ENST00000394867.8:c.756-161_756-158del	ENSP00000378336.1:n.756-161_756-158del
ENST00000597263.5:n.232-161_232-158del
ENST00000599021.1:c.157-161_157-158del
ENST00000600584.5:n.2335_2338del
ENST00000601786.5:n.1348-161_1348-158del
NM_030662.3:c.1047-161_1047-158del , LRG_750t1:c.1047-161_1047-158del	NP_109587.1:n.1047-161_1047-158del
XM_006722799.2:c.768-161_768-158del	XP_006722862.1:n.768-161_768-158del
XM_011528133.1:c.477-161_477-158del	XP_011526435.1:n.477-161_477-158del
XM_017026989.1:c.1434_1437del	XP_016882478.1:p.Gly479AlafsTer?
XM_017026990.1:c.1155_1158del	XP_016882479.1:p.Gly386AlafsTer?
NM_030662.4:c.1047-161_1047-158del MANE Select	NP_109587.1:n.1047-161_1047-158del