Canonical Allele Identifier: CA2319222166

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040901008

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095291_4095327del , CM000681.2:g.4095291_4095327del	GRCh38
NC_000019.9:g.4095289_4095325del , CM000681.1:g.4095289_4095325del	GRCh37
NC_000019.8:g.4046289_4046325del	NCBI36
NG_007996.1:g.33803_33839del , LRG_750:g.33803_33839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+62_1485+98del
ENST00000688002.1:n.3197+62_3197+98del
ENST00000688751.1:n.182+62_182+98del
ENST00000689792.1:n.950+62_950+98del
ENST00000262948.10:c.1046+62_1046+98del MANE Select	ENSP00000262948.4:n.1046+62_1046+98del
ENST00000262948.9:c.1046+62_1046+98del	ENSP00000262948.3:n.1046+62_1046+98del
ENST00000394867.8:c.755+62_755+98del	ENSP00000378336.1:n.755+62_755+98del
ENST00000597263.5:n.231+62_231+98del
ENST00000599021.1:c.156+62_156+98del
ENST00000600584.5:n.1668_1704del
ENST00000601786.5:n.1347+62_1347+98del
NM_030662.3:c.1046+62_1046+98del , LRG_750t1:c.1046+62_1046+98del	NP_109587.1:n.1046+62_1046+98del
XM_006722799.2:c.767+62_767+98del	XP_006722862.1:n.767+62_767+98del
XM_011528133.1:c.476+62_476+98del	XP_011526435.1:n.476+62_476+98del
XM_017026989.1:c.1046+62_1046+98del	XP_016882478.1:n.1046+62_1046+98del
XM_017026990.1:c.767+62_767+98del	XP_016882479.1:n.767+62_767+98del
NM_030662.4:c.1046+62_1046+98del MANE Select	NP_109587.1:n.1046+62_1046+98del