Canonical Allele Identifier: CA2576573181

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099169-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099171del , CM000681.2:g.4099171del	GRCh38
NC_000019.9:g.4099169del , CM000681.1:g.4099169del	GRCh37
NC_000019.8:g.4050169del	NCBI36
NG_007996.1:g.29959del , LRG_750:g.29959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+31del
ENST00000687128.1:n.1389del
ENST00000688002.1:n.1244del
ENST00000689792.1:n.823+31del
ENST00000262948.10:c.919+31del MANE Select	ENSP00000262948.4:n.919+31del
ENST00000262948.9:c.919+31del	ENSP00000262948.3:n.919+31del
ENST00000394867.8:c.628+31del	ENSP00000378336.1:n.628+31del
ENST00000595715.1:n.734+31del
ENST00000597263.5:n.169+1849del
ENST00000599021.1:c.30-1827del
ENST00000600584.5:n.1479+31del
ENST00000601786.5:n.1220+31del
NM_030662.3:c.919+31del , LRG_750t1:c.919+31del	NP_109587.1:n.919+31del
XM_006722799.2:c.705+1849del	XP_006722862.1:n.705+1849del
XM_011528133.1:c.349+31del	XP_011526435.1:n.349+31del
XM_017026989.1:c.919+31del	XP_016882478.1:n.919+31del
XM_017026990.1:c.705+1849del	XP_016882479.1:n.705+1849del
NM_030662.4:c.919+31del MANE Select	NP_109587.1:n.919+31del