Canonical Allele Identifier: CA631538299

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1324541440
• gnomAD v2: 19-4095645-GGAAA-G
• MyVariant Identifiers: chr19:g.4095646_4095649del (hg19) ; chr19:g.4095648_4095651del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095650_4095653del , CM000681.2:g.4095650_4095653del	GRCh38
NC_000019.9:g.4095648_4095651del , CM000681.1:g.4095648_4095651del	GRCh37
NC_000019.8:g.4046648_4046651del	NCBI36
NG_007996.1:g.33478_33481del , LRG_750:g.33478_33481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-202_1424-199del
ENST00000688002.1:n.3136-202_3136-199del
ENST00000688751.1:n.121-202_121-199del
ENST00000689792.1:n.889-202_889-199del
ENST00000262948.10:c.985-202_985-199del MANE Select	ENSP00000262948.4:n.985-202_985-199del
ENST00000262948.9:c.985-202_985-199del	ENSP00000262948.3:n.985-202_985-199del
ENST00000394867.8:c.694-202_694-199del	ENSP00000378336.1:n.694-202_694-199del
ENST00000595715.1:n.800-202_800-199del
ENST00000597263.5:n.170-202_170-199del
ENST00000599021.1:c.95-202_95-199del
ENST00000600584.5:n.1545-202_1545-199del
ENST00000601786.5:n.1286-202_1286-199del
NM_030662.3:c.985-202_985-199del , LRG_750t1:c.985-202_985-199del	NP_109587.1:n.985-202_985-199del
XM_006722799.2:c.706-202_706-199del	XP_006722862.1:n.706-202_706-199del
XM_011528133.1:c.415-202_415-199del	XP_011526435.1:n.415-202_415-199del
XM_017026989.1:c.985-202_985-199del	XP_016882478.1:n.985-202_985-199del
XM_017026990.1:c.706-202_706-199del	XP_016882479.1:n.706-202_706-199del
NM_030662.4:c.985-202_985-199del MANE Select	NP_109587.1:n.985-202_985-199del