Canonical Allele Identifier: CA631538297

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1407304558
• gnomAD v2: 19-4095640-TAGAGGG-T
• gnomAD v3: 19-4095642-TAGAGGG-T
• gnomAD v4: 19-4095642-TAGAGGG-T
• MyVariant Identifiers: chr19:g.4095641_4095646del (hg19) ; chr19:g.4095643_4095648del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095644_4095649del , CM000681.2:g.4095644_4095649del	GRCh38
NC_000019.9:g.4095642_4095647del , CM000681.1:g.4095642_4095647del	GRCh37
NC_000019.8:g.4046642_4046647del	NCBI36
NG_007996.1:g.33481_33486del , LRG_750:g.33481_33486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-199_1424-194del
ENST00000688002.1:n.3136-199_3136-194del
ENST00000688751.1:n.121-199_121-194del
ENST00000689792.1:n.889-199_889-194del
ENST00000262948.10:c.985-199_985-194del MANE Select	ENSP00000262948.4:n.985-199_985-194del
ENST00000262948.9:c.985-199_985-194del	ENSP00000262948.3:n.985-199_985-194del
ENST00000394867.8:c.694-199_694-194del	ENSP00000378336.1:n.694-199_694-194del
ENST00000595715.1:n.800-199_800-194del
ENST00000597263.5:n.170-199_170-194del
ENST00000599021.1:c.95-199_95-194del
ENST00000600584.5:n.1545-199_1545-194del
ENST00000601786.5:n.1286-199_1286-194del
NM_030662.3:c.985-199_985-194del , LRG_750t1:c.985-199_985-194del	NP_109587.1:n.985-199_985-194del
XM_006722799.2:c.706-199_706-194del	XP_006722862.1:n.706-199_706-194del
XM_011528133.1:c.415-199_415-194del	XP_011526435.1:n.415-199_415-194del
XM_017026989.1:c.985-199_985-194del	XP_016882478.1:n.985-199_985-194del
XM_017026990.1:c.706-199_706-194del	XP_016882479.1:n.706-199_706-194del
NM_030662.4:c.985-199_985-194del MANE Select	NP_109587.1:n.985-199_985-194del