Canonical Allele Identifier: CA2584878326

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099150-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099154_4099155del , CM000681.2:g.4099154_4099155del	GRCh38
NC_000019.9:g.4099152_4099153del , CM000681.1:g.4099152_4099153del	GRCh37
NC_000019.8:g.4050152_4050153del	NCBI36
NG_007996.1:g.29977_29978del , LRG_750:g.29977_29978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+49_1358+50del
ENST00000687128.1:n.1407_1408del
ENST00000688002.1:n.1262_1263del
ENST00000689792.1:n.823+49_823+50del
ENST00000262948.10:c.919+49_919+50del MANE Select	ENSP00000262948.4:n.919+49_919+50del
ENST00000262948.9:c.919+49_919+50del	ENSP00000262948.3:n.919+49_919+50del
ENST00000394867.8:c.628+49_628+50del	ENSP00000378336.1:n.628+49_628+50del
ENST00000595715.1:n.734+49_734+50del
ENST00000597263.5:n.169+1867_169+1868del
ENST00000599021.1:c.30-1809_30-1808del
ENST00000600584.5:n.1479+49_1479+50del
ENST00000601786.5:n.1220+49_1220+50del
NM_030662.3:c.919+49_919+50del , LRG_750t1:c.919+49_919+50del	NP_109587.1:n.919+49_919+50del
XM_006722799.2:c.705+1867_705+1868del	XP_006722862.1:n.705+1867_705+1868del
XM_011528133.1:c.349+49_349+50del	XP_011526435.1:n.349+49_349+50del
XM_017026989.1:c.919+49_919+50del	XP_016882478.1:n.919+49_919+50del
XM_017026990.1:c.705+1867_705+1868del	XP_016882479.1:n.705+1867_705+1868del
NM_030662.4:c.919+49_919+50del MANE Select	NP_109587.1:n.919+49_919+50del