Canonical Allele Identifier: CA882242000

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1156545162
• gnomAD v3: 19-4095461-A-AACAGAG
• gnomAD v4: 19-4095461-A-AACAGAG
• MyVariant Identifiers: chr19:g.4095459_4095460insACAGAG (hg19) ; chr19:g.4095461_4095462insACAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095462_4095467dup , CM000681.2:g.4095462_4095467dup	GRCh38
NC_000019.9:g.4095460_4095465dup , CM000681.1:g.4095460_4095465dup	GRCh37
NC_000019.8:g.4046460_4046465dup	NCBI36
NG_007996.1:g.33662_33667dup , LRG_750:g.33662_33667dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-18_1424-13dup
ENST00000688002.1:n.3136-18_3136-13dup
ENST00000688751.1:n.121-18_121-13dup
ENST00000689792.1:n.889-18_889-13dup
ENST00000262948.10:c.985-18_985-13dup MANE Select	ENSP00000262948.4:n.985-18_985-13dup
ENST00000262948.9:c.985-18_985-13dup	ENSP00000262948.3:n.985-18_985-13dup
ENST00000394867.8:c.694-18_694-13dup	ENSP00000378336.1:n.694-18_694-13dup
ENST00000595715.1:n.800-18_800-13dup
ENST00000597263.5:n.170-18_170-13dup
ENST00000599021.1:c.95-18_95-13dup
ENST00000600584.5:n.1545-18_1545-13dup
ENST00000601786.5:n.1286-18_1286-13dup
NM_030662.3:c.985-18_985-13dup , LRG_750t1:c.985-18_985-13dup	NP_109587.1:n.985-18_985-13dup
XM_006722799.2:c.706-18_706-13dup	XP_006722862.1:n.706-18_706-13dup
XM_011528133.1:c.415-18_415-13dup	XP_011526435.1:n.415-18_415-13dup
XM_017026989.1:c.985-18_985-13dup	XP_016882478.1:n.985-18_985-13dup
XM_017026990.1:c.706-18_706-13dup	XP_016882479.1:n.706-18_706-13dup
NM_030662.4:c.985-18_985-13dup MANE Select	NP_109587.1:n.985-18_985-13dup