Canonical Allele Identifier: CA2584877865

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095362-GGTGTGGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095363_4095370del , CM000681.2:g.4095363_4095370del	GRCh38
NC_000019.9:g.4095361_4095368del , CM000681.1:g.4095361_4095368del	GRCh37
NC_000019.8:g.4046361_4046368del	NCBI36
NG_007996.1:g.33759_33766del , LRG_750:g.33759_33766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+18_1485+25del
ENST00000688002.1:n.3197+18_3197+25del
ENST00000688751.1:n.182+18_182+25del
ENST00000689792.1:n.950+18_950+25del
ENST00000262948.10:c.1046+18_1046+25del MANE Select	ENSP00000262948.4:n.1046+18_1046+25del
ENST00000262948.9:c.1046+18_1046+25del	ENSP00000262948.3:n.1046+18_1046+25del
ENST00000394867.8:c.755+18_755+25del	ENSP00000378336.1:n.755+18_755+25del
ENST00000597263.5:n.231+18_231+25del
ENST00000599021.1:c.156+18_156+25del
ENST00000600584.5:n.1624_1631del
ENST00000601786.5:n.1347+18_1347+25del
NM_030662.3:c.1046+18_1046+25del , LRG_750t1:c.1046+18_1046+25del	NP_109587.1:n.1046+18_1046+25del
XM_006722799.2:c.767+18_767+25del	XP_006722862.1:n.767+18_767+25del
XM_011528133.1:c.476+18_476+25del	XP_011526435.1:n.476+18_476+25del
XM_017026989.1:c.1046+18_1046+25del	XP_016882478.1:n.1046+18_1046+25del
XM_017026990.1:c.767+18_767+25del	XP_016882479.1:n.767+18_767+25del
NM_030662.4:c.1046+18_1046+25del MANE Select	NP_109587.1:n.1046+18_1046+25del