Canonical Allele Identifier: CA882244268

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1206257638
• MyVariant Identifiers: chr19:g.4099480del (hg19) ; chr19:g.4099482del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099485del , CM000681.2:g.4099485del	GRCh38
NC_000019.9:g.4099483del , CM000681.1:g.4099483del	GRCh37
NC_000019.8:g.4050483del	NCBI36
NG_007996.1:g.29647del , LRG_750:g.29647del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-68del
ENST00000687128.1:n.1145-68del
ENST00000688002.1:n.932del
ENST00000689792.1:n.646-104del
ENST00000262948.10:c.706-68del MANE Select	ENSP00000262948.4:n.706-68del
ENST00000262948.9:c.706-68del	ENSP00000262948.3:n.706-68del
ENST00000394867.8:c.415-68del	ENSP00000378336.1:n.415-68del
ENST00000593364.5:n.653-68del
ENST00000595715.1:n.453del
ENST00000597263.5:n.169+1537del
ENST00000599021.1:c.29+1537del
ENST00000600584.5:n.1198del
ENST00000601786.5:n.1007-68del
ENST00000602167.5:n.426-68del
NM_030662.3:c.706-68del , LRG_750t1:c.706-68del	NP_109587.1:n.706-68del
XM_006722799.2:c.705+1537del	XP_006722862.1:n.705+1537del
XM_011528133.1:c.136-68del	XP_011526435.1:n.136-68del
XM_017026989.1:c.706-68del	XP_016882478.1:n.706-68del
XM_017026990.1:c.705+1537del	XP_016882479.1:n.705+1537del
XM_017026991.1:c.*248del	XP_016882480.1:n.*248del
NM_030662.4:c.706-68del MANE Select	NP_109587.1:n.706-68del