Canonical Allele Identifier: CA2584877817

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095291-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095293del , CM000681.2:g.4095293del	GRCh38
NC_000019.9:g.4095291del , CM000681.1:g.4095291del	GRCh37
NC_000019.8:g.4046291del	NCBI36
NG_007996.1:g.33837del , LRG_750:g.33837del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+96del
ENST00000688002.1:n.3197+96del
ENST00000688751.1:n.182+96del
ENST00000689792.1:n.950+96del
ENST00000262948.10:c.1046+96del MANE Select	ENSP00000262948.4:n.1046+96del
ENST00000262948.9:c.1046+96del	ENSP00000262948.3:n.1046+96del
ENST00000394867.8:c.755+96del	ENSP00000378336.1:n.755+96del
ENST00000597263.5:n.231+96del
ENST00000599021.1:c.156+96del
ENST00000600584.5:n.1702del
ENST00000601786.5:n.1347+96del
NM_030662.3:c.1046+96del , LRG_750t1:c.1046+96del	NP_109587.1:n.1046+96del
XM_006722799.2:c.767+96del	XP_006722862.1:n.767+96del
XM_011528133.1:c.476+96del	XP_011526435.1:n.476+96del
XM_017026989.1:c.1046+96del	XP_016882478.1:n.1046+96del
XM_017026990.1:c.767+96del	XP_016882479.1:n.767+96del
NM_030662.4:c.1046+96del MANE Select	NP_109587.1:n.1046+96del