Canonical Allele Identifier: CA2319219718

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090579_4090580delinsGC , CM000681.2:g.4090579_4090580delinsGC	GRCh38
NC_000019.9:g.4090577_4090578delinsGC , CM000681.1:g.4090577_4090578delinsGC	GRCh37
NC_000019.8:g.4041577_4041578delinsGC	NCBI36
NG_007996.1:g.38549_38550delinsGC , LRG_750:g.38549_38550delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1660_1661delinsGC
ENST00000688002.1:n.3372_3373delinsGC
ENST00000688751.1:n.357_358delinsGC
ENST00000689792.1:n.1125_1126delinsGC
ENST00000262948.10:c.*18_*19delinsGC MANE Select	ENSP00000262948.4:n.*18_*19delinsGC
ENST00000262948.9:c.*18_*19delinsGC	ENSP00000262948.3:n.*18_*19delinsGC
ENST00000394867.8:c.*18_*19delinsGC	ENSP00000378336.1:n.*18_*19delinsGC
ENST00000597263.5:n.406_407delinsGC
ENST00000600584.5:n.2670_2671delinsGC
ENST00000601786.5:n.1522_1523delinsGC
NM_030662.3:c.*18_*19delinsGC , LRG_750t1:c.*18_*19delinsGC	NP_109587.1:n.*18_*19delinsGC
XM_006722799.2:c.*18_*19delinsGC	XP_006722862.1:n.*18_*19delinsGC
XM_011528133.1:c.*18_*19delinsGC	XP_011526435.1:n.*18_*19delinsGC
NM_030662.4:c.*18_*19delinsGC MANE Select	NP_109587.1:n.*18_*19delinsGC