Canonical Allele Identifier: CA2697555625

Gene: MAP2K2

Linked Data

• ClinVar Variation Id: 2709681
• ClinVar RCV Id: RCV003539635

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095465G>T , CM000681.2:g.4095465G>T	GRCh38
NC_000019.9:g.4095463G>T , CM000681.1:g.4095463G>T	GRCh37
NC_000019.8:g.4046463G>T	NCBI36
NG_007996.1:g.33664C>A , LRG_750:g.33664C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-16C>A
ENST00000688002.1:n.3136-16C>A
ENST00000688751.1:n.121-16C>A
ENST00000689792.1:n.889-16C>A
ENST00000262948.10:c.985-16C>A MANE Select	ENSP00000262948.4:n.985-16C>A
ENST00000262948.9:c.985-16C>A	ENSP00000262948.3:n.985-16C>A
ENST00000394867.8:c.694-16C>A	ENSP00000378336.1:n.694-16C>A
ENST00000595715.1:n.800-16C>A
ENST00000597263.5:n.170-16C>A
ENST00000599021.1:c.95-16C>A
ENST00000600584.5:n.1545-16C>A
ENST00000601786.5:n.1286-16C>A
NM_030662.3:c.985-16C>A , LRG_750t1:c.985-16C>A	NP_109587.1:n.985-16C>A
XM_006722799.2:c.706-16C>A	XP_006722862.1:n.706-16C>A
XM_011528133.1:c.415-16C>A	XP_011526435.1:n.415-16C>A
XM_017026989.1:c.985-16C>A	XP_016882478.1:n.985-16C>A
XM_017026990.1:c.706-16C>A	XP_016882479.1:n.706-16C>A
NM_030662.4:c.985-16C>A MANE Select	NP_109587.1:n.985-16C>A