Canonical Allele Identifier: CA631538283

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1449547536
• gnomAD v2: 19-4095587-CCT-C
• gnomAD v3: 19-4095589-CCT-C
• gnomAD v4: 19-4095589-CCT-C
• MyVariant Identifiers: chr19:g.4095588_4095589del (hg19) ; chr19:g.4095590_4095591del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095590_4095591del , CM000681.2:g.4095590_4095591del	GRCh38
NC_000019.9:g.4095588_4095589del , CM000681.1:g.4095588_4095589del	GRCh37
NC_000019.8:g.4046588_4046589del	NCBI36
NG_007996.1:g.33538_33539del , LRG_750:g.33538_33539del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-142_1424-141del
ENST00000688002.1:n.3136-142_3136-141del
ENST00000688751.1:n.121-142_121-141del
ENST00000689792.1:n.889-142_889-141del
ENST00000262948.10:c.985-142_985-141del MANE Select	ENSP00000262948.4:n.985-142_985-141del
ENST00000262948.9:c.985-142_985-141del	ENSP00000262948.3:n.985-142_985-141del
ENST00000394867.8:c.694-142_694-141del	ENSP00000378336.1:n.694-142_694-141del
ENST00000595715.1:n.800-142_800-141del
ENST00000597263.5:n.170-142_170-141del
ENST00000599021.1:c.95-142_95-141del
ENST00000600584.5:n.1545-142_1545-141del
ENST00000601786.5:n.1286-142_1286-141del
NM_030662.3:c.985-142_985-141del , LRG_750t1:c.985-142_985-141del	NP_109587.1:n.985-142_985-141del
XM_006722799.2:c.706-142_706-141del	XP_006722862.1:n.706-142_706-141del
XM_011528133.1:c.415-142_415-141del	XP_011526435.1:n.415-142_415-141del
XM_017026989.1:c.985-142_985-141del	XP_016882478.1:n.985-142_985-141del
XM_017026990.1:c.706-142_706-141del	XP_016882479.1:n.706-142_706-141del
NM_030662.4:c.985-142_985-141del MANE Select	NP_109587.1:n.985-142_985-141del