Canonical Allele Identifier: CA882244272

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1211032613
• gnomAD v3: 19-4099488-T-TAA
• gnomAD v4: 19-4099488-T-TAA
• MyVariant Identifiers: chr19:g.4099486_4099487insAA (hg19) ; chr19:g.4099488_4099489insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099489_4099490insAA , CM000681.2:g.4099489_4099490insAA	GRCh38
NC_000019.9:g.4099487_4099488insAA , CM000681.1:g.4099487_4099488insAA	GRCh37
NC_000019.8:g.4050487_4050488insAA	NCBI36
NG_007996.1:g.29640_29641insTT , LRG_750:g.29640_29641insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-75_1145-74insTT
ENST00000687128.1:n.1145-75_1145-74insTT
ENST00000688002.1:n.925_926insTT
ENST00000689792.1:n.646-111_646-110insTT
ENST00000262948.10:c.706-75_706-74insTT MANE Select	ENSP00000262948.4:n.706-75_706-74insTT
ENST00000262948.9:c.706-75_706-74insTT	ENSP00000262948.3:n.706-75_706-74insTT
ENST00000394867.8:c.415-75_415-74insTT	ENSP00000378336.1:n.415-75_415-74insTT
ENST00000593364.5:n.653-75_653-74insTT
ENST00000595715.1:n.446_447insTT
ENST00000597263.5:n.169+1530_169+1531insTT
ENST00000599021.1:c.29+1530_29+1531insTT
ENST00000600584.5:n.1191_1192insTT
ENST00000601786.5:n.1007-75_1007-74insTT
ENST00000602167.5:n.426-75_426-74insTT
NM_030662.3:c.706-75_706-74insTT , LRG_750t1:c.706-75_706-74insTT	NP_109587.1:n.706-75_706-74insTT
XM_006722799.2:c.705+1530_705+1531insTT	XP_006722862.1:n.705+1530_705+1531insTT
XM_011528133.1:c.136-75_136-74insTT	XP_011526435.1:n.136-75_136-74insTT
XM_017026989.1:c.706-75_706-74insTT	XP_016882478.1:n.706-75_706-74insTT
XM_017026990.1:c.705+1530_705+1531insTT	XP_016882479.1:n.705+1530_705+1531insTT
XM_017026991.1:c.*241_*242insTT	XP_016882480.1:n.*241_*242insTT
NM_030662.4:c.706-75_706-74insTT MANE Select	NP_109587.1:n.706-75_706-74insTT