Canonical Allele Identifier: CA2584877180

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094724-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094726_4094727del , CM000681.2:g.4094726_4094727del	GRCh38
NC_000019.9:g.4094724_4094725del , CM000681.1:g.4094724_4094725del	GRCh37
NC_000019.8:g.4045724_4045725del	NCBI36
NG_007996.1:g.34403_34404del , LRG_750:g.34403_34404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-228_1486-227del
ENST00000688002.1:n.3198-228_3198-227del
ENST00000688751.1:n.183-228_183-227del
ENST00000689792.1:n.951-228_951-227del
ENST00000262948.10:c.1047-228_1047-227del MANE Select	ENSP00000262948.4:n.1047-228_1047-227del
ENST00000262948.9:c.1047-228_1047-227del	ENSP00000262948.3:n.1047-228_1047-227del
ENST00000394867.8:c.756-228_756-227del	ENSP00000378336.1:n.756-228_756-227del
ENST00000597263.5:n.232-228_232-227del
ENST00000599021.1:c.157-228_157-227del
ENST00000600584.5:n.2268_2269del
ENST00000601786.5:n.1348-228_1348-227del
NM_030662.3:c.1047-228_1047-227del , LRG_750t1:c.1047-228_1047-227del	NP_109587.1:n.1047-228_1047-227del
XM_006722799.2:c.768-228_768-227del	XP_006722862.1:n.768-228_768-227del
XM_011528133.1:c.477-228_477-227del	XP_011526435.1:n.477-228_477-227del
XM_017026989.1:c.1367_1368del	XP_016882478.1:p.His456ProfsTer?
XM_017026990.1:c.1088_1089del	XP_016882479.1:p.His363ProfsTer?
NM_030662.4:c.1047-228_1047-227del MANE Select	NP_109587.1:n.1047-228_1047-227del