Canonical Allele Identifier: CA304449073

Gene: MAP2K2

Linked Data

• dbSNP Id: rs772903129
• gnomAD v3: 19-4098994-GACAGA-G
• gnomAD v4: 19-4098994-GACAGA-G
• MyVariant Identifiers: chr19:g.4098993_4098997del (hg19) ; chr19:g.4098995_4098999del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4098999_4099003del , CM000681.2:g.4098999_4099003del	GRCh38
NC_000019.9:g.4098997_4099001del , CM000681.1:g.4098997_4099001del	GRCh37
NC_000019.8:g.4049997_4050001del	NCBI36
NG_007996.1:g.30130_30134del , LRG_750:g.30130_30134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+202_1358+206del
ENST00000687128.1:n.1560_1564del
ENST00000688002.1:n.1415_1419del
ENST00000689792.1:n.823+202_823+206del
ENST00000262948.10:c.919+202_919+206del MANE Select	ENSP00000262948.4:n.919+202_919+206del
ENST00000262948.9:c.919+202_919+206del	ENSP00000262948.3:n.919+202_919+206del
ENST00000394867.8:c.628+202_628+206del	ENSP00000378336.1:n.628+202_628+206del
ENST00000595715.1:n.734+202_734+206del
ENST00000597263.5:n.169+2020_169+2024del
ENST00000599021.1:c.30-1656_30-1652del
ENST00000600584.5:n.1479+202_1479+206del
ENST00000601786.5:n.1220+202_1220+206del
NM_030662.3:c.919+202_919+206del , LRG_750t1:c.919+202_919+206del	NP_109587.1:n.919+202_919+206del
XM_006722799.2:c.705+2020_705+2024del	XP_006722862.1:n.705+2020_705+2024del
XM_011528133.1:c.349+202_349+206del	XP_011526435.1:n.349+202_349+206del
XM_017026989.1:c.919+202_919+206del	XP_016882478.1:n.919+202_919+206del
XM_017026990.1:c.705+2020_705+2024del	XP_016882479.1:n.705+2020_705+2024del
NM_030662.4:c.919+202_919+206del MANE Select	NP_109587.1:n.919+202_919+206del