Canonical Allele Identifier: CA2584877050

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094604-CTGGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094605_4094609del , CM000681.2:g.4094605_4094609del	GRCh38
NC_000019.9:g.4094603_4094607del , CM000681.1:g.4094603_4094607del	GRCh37
NC_000019.8:g.4045603_4045607del	NCBI36
NG_007996.1:g.34520_34524del , LRG_750:g.34520_34524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-111_1486-107del
ENST00000688002.1:n.3198-111_3198-107del
ENST00000688751.1:n.183-111_183-107del
ENST00000689792.1:n.951-111_951-107del
ENST00000262948.10:c.1047-111_1047-107del MANE Select	ENSP00000262948.4:n.1047-111_1047-107del
ENST00000262948.9:c.1047-111_1047-107del	ENSP00000262948.3:n.1047-111_1047-107del
ENST00000394867.8:c.756-111_756-107del	ENSP00000378336.1:n.756-111_756-107del
ENST00000597263.5:n.232-111_232-107del
ENST00000599021.1:c.157-111_157-107del
ENST00000600584.5:n.2385_2389del
ENST00000601786.5:n.1348-111_1348-107del
NM_030662.3:c.1047-111_1047-107del , LRG_750t1:c.1047-111_1047-107del	NP_109587.1:n.1047-111_1047-107del
XM_006722799.2:c.768-111_768-107del	XP_006722862.1:n.768-111_768-107del
XM_011528133.1:c.477-111_477-107del	XP_011526435.1:n.477-111_477-107del
XM_017026989.1:c.1484_1488del	XP_016882478.1:p.Asp495GlyfsTer?
XM_017026990.1:c.1205_1209del	XP_016882479.1:p.Asp402GlyfsTer?
NM_030662.4:c.1047-111_1047-107del MANE Select	NP_109587.1:n.1047-111_1047-107del