Canonical Allele Identifier: CA2584877787

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095266-CCTGCCTAACG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095271_4095280del , CM000681.2:g.4095271_4095280del	GRCh38
NC_000019.9:g.4095269_4095278del , CM000681.1:g.4095269_4095278del	GRCh37
NC_000019.8:g.4046269_4046278del	NCBI36
NG_007996.1:g.33853_33862del , LRG_750:g.33853_33862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+112_1485+121del
ENST00000688002.1:n.3197+112_3197+121del
ENST00000688751.1:n.182+112_182+121del
ENST00000689792.1:n.950+112_950+121del
ENST00000262948.10:c.1046+112_1046+121del MANE Select	ENSP00000262948.4:n.1046+112_1046+121del
ENST00000262948.9:c.1046+112_1046+121del	ENSP00000262948.3:n.1046+112_1046+121del
ENST00000394867.8:c.755+112_755+121del	ENSP00000378336.1:n.755+112_755+121del
ENST00000597263.5:n.231+112_231+121del
ENST00000599021.1:c.156+112_156+121del
ENST00000600584.5:n.1718_1727del
ENST00000601786.5:n.1347+112_1347+121del
NM_030662.3:c.1046+112_1046+121del , LRG_750t1:c.1046+112_1046+121del	NP_109587.1:n.1046+112_1046+121del
XM_006722799.2:c.767+112_767+121del	XP_006722862.1:n.767+112_767+121del
XM_011528133.1:c.476+112_476+121del	XP_011526435.1:n.476+112_476+121del
XM_017026989.1:c.1046+112_1046+121del	XP_016882478.1:n.1046+112_1046+121del
XM_017026990.1:c.767+112_767+121del	XP_016882479.1:n.767+112_767+121del
NM_030662.4:c.1046+112_1046+121del MANE Select	NP_109587.1:n.1046+112_1046+121del