Canonical Allele Identifier: CA9090719

Gene: MAP2K2

Linked Data

• dbSNP Id: rs765808369
• ExAC: 19:4094530 TGGA / T
• gnomAD v2: 19-4094530-TGGA-T
• gnomAD v3: 19-4094532-TGGA-T
• gnomAD v4: 19-4094532-TGGA-T
• MyVariant Identifiers: chr19:g.4094531_4094533del (hg19) ; chr19:g.4094533_4094535del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094537_4094539del , CM000681.2:g.4094537_4094539del	GRCh38
NC_000019.9:g.4094535_4094537del , CM000681.1:g.4094535_4094537del	GRCh37
NC_000019.8:g.4045535_4045537del	NCBI36
NG_007996.1:g.34594_34596del , LRG_750:g.34594_34596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-37_1486-35del
ENST00000688002.1:n.3198-37_3198-35del
ENST00000688751.1:n.183-37_183-35del
ENST00000689792.1:n.951-37_951-35del
ENST00000262948.10:c.1047-37_1047-35del MANE Select	ENSP00000262948.4:n.1047-37_1047-35del
ENST00000262948.9:c.1047-37_1047-35del	ENSP00000262948.3:n.1047-37_1047-35del
ENST00000394867.8:c.756-37_756-35del	ENSP00000378336.1:n.756-37_756-35del
ENST00000597263.5:n.232-37_232-35del
ENST00000599021.1:c.157-37_157-35del
ENST00000600584.5:n.2459_2461del
ENST00000601786.5:n.1348-37_1348-35del
NM_030662.3:c.1047-37_1047-35del , LRG_750t1:c.1047-37_1047-35del	NP_109587.1:n.1047-37_1047-35del
XM_006722799.2:c.768-37_768-35del	XP_006722862.1:n.768-37_768-35del
XM_011528133.1:c.477-37_477-35del	XP_011526435.1:n.477-37_477-35del
XM_017026989.1:c.*19_*21del	XP_016882478.1:n.*19_*21del
XM_017026990.1:c.*19_*21del	XP_016882479.1:n.*19_*21del
NM_030662.4:c.1047-37_1047-35del MANE Select	NP_109587.1:n.1047-37_1047-35del