Canonical Allele Identifier: CA882241835

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1418513409
• MyVariant Identifiers: chr19:g.4094629_4094630del (hg19) ; chr19:g.4094631_4094632del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094633_4094634del , CM000681.2:g.4094633_4094634del	GRCh38
NC_000019.9:g.4094631_4094632del , CM000681.1:g.4094631_4094632del	GRCh37
NC_000019.8:g.4045631_4045632del	NCBI36
NG_007996.1:g.34497_34498del , LRG_750:g.34497_34498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-134_1486-133del
ENST00000688002.1:n.3198-134_3198-133del
ENST00000688751.1:n.183-134_183-133del
ENST00000689792.1:n.951-134_951-133del
ENST00000262948.10:c.1047-134_1047-133del MANE Select	ENSP00000262948.4:n.1047-134_1047-133del
ENST00000262948.9:c.1047-134_1047-133del	ENSP00000262948.3:n.1047-134_1047-133del
ENST00000394867.8:c.756-134_756-133del	ENSP00000378336.1:n.756-134_756-133del
ENST00000597263.5:n.232-134_232-133del
ENST00000599021.1:c.157-134_157-133del
ENST00000600584.5:n.2362_2363del
ENST00000601786.5:n.1348-134_1348-133del
NM_030662.3:c.1047-134_1047-133del , LRG_750t1:c.1047-134_1047-133del	NP_109587.1:n.1047-134_1047-133del
XM_006722799.2:c.768-134_768-133del	XP_006722862.1:n.768-134_768-133del
XM_011528133.1:c.477-134_477-133del	XP_011526435.1:n.477-134_477-133del
XM_017026989.1:c.1461_1462del	XP_016882478.1:p.Ala488HisfsTer?
XM_017026990.1:c.1182_1183del	XP_016882479.1:p.Ala395HisfsTer?
NM_030662.4:c.1047-134_1047-133del MANE Select	NP_109587.1:n.1047-134_1047-133del