Canonical Allele Identifier: CA2319224244

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099023_4099024delinsTC , CM000681.2:g.4099023_4099024delinsTC	GRCh38
NC_000019.9:g.4099021_4099022delinsTC , CM000681.1:g.4099021_4099022delinsTC	GRCh37
NC_000019.8:g.4050021_4050022delinsTC	NCBI36
NG_007996.1:g.30105_30106delinsGA , LRG_750:g.30105_30106delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+177_1358+178delinsGA
ENST00000687128.1:n.1535_1536delinsGA
ENST00000688002.1:n.1390_1391delinsGA
ENST00000689792.1:n.823+177_823+178delinsGA
ENST00000262948.10:c.919+177_919+178delinsGA MANE Select	ENSP00000262948.4:n.919+177_919+178delinsGA
ENST00000262948.9:c.919+177_919+178delinsGA	ENSP00000262948.3:n.919+177_919+178delinsGA
ENST00000394867.8:c.628+177_628+178delinsGA	ENSP00000378336.1:n.628+177_628+178delinsGA
ENST00000595715.1:n.734+177_734+178delinsGA
ENST00000597263.5:n.169+1995_169+1996delinsGA
ENST00000599021.1:c.30-1681_30-1680delinsGA
ENST00000600584.5:n.1479+177_1479+178delinsGA
ENST00000601786.5:n.1220+177_1220+178delinsGA
NM_030662.3:c.919+177_919+178delinsGA , LRG_750t1:c.919+177_919+178delinsGA	NP_109587.1:n.919+177_919+178delinsGA
XM_006722799.2:c.705+1995_705+1996delinsGA	XP_006722862.1:n.705+1995_705+1996delinsGA
XM_011528133.1:c.349+177_349+178delinsGA	XP_011526435.1:n.349+177_349+178delinsGA
XM_017026989.1:c.919+177_919+178delinsGA	XP_016882478.1:n.919+177_919+178delinsGA
XM_017026990.1:c.705+1995_705+1996delinsGA	XP_016882479.1:n.705+1995_705+1996delinsGA
NM_030662.4:c.919+177_919+178delinsGA MANE Select	NP_109587.1:n.919+177_919+178delinsGA