Canonical Allele Identifier: CA304449061

Gene: MAP2K2

Linked Data

• dbSNP Id: rs747759118
• gnomAD v3: 19-4098982-GC-G
• gnomAD v4: 19-4098982-GC-G
• MyVariant Identifiers: chr19:g.4098981del (hg19) ; chr19:g.4098983del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4098983del , CM000681.2:g.4098983del	GRCh38
NC_000019.9:g.4098981del , CM000681.1:g.4098981del	GRCh37
NC_000019.8:g.4049981del	NCBI36
NG_007996.1:g.30146del , LRG_750:g.30146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+218del
ENST00000687128.1:n.1576del
ENST00000688002.1:n.1431del
ENST00000689792.1:n.823+218del
ENST00000262948.10:c.919+218del MANE Select	ENSP00000262948.4:n.919+218del
ENST00000262948.9:c.919+218del	ENSP00000262948.3:n.919+218del
ENST00000394867.8:c.628+218del	ENSP00000378336.1:n.628+218del
ENST00000595715.1:n.734+218del
ENST00000597263.5:n.169+2036del
ENST00000599021.1:c.30-1640del
ENST00000600584.5:n.1479+218del
ENST00000601786.5:n.1220+218del
NM_030662.3:c.919+218del , LRG_750t1:c.919+218del	NP_109587.1:n.919+218del
XM_006722799.2:c.705+2036del	XP_006722862.1:n.705+2036del
XM_011528133.1:c.349+218del	XP_011526435.1:n.349+218del
XM_017026989.1:c.919+218del	XP_016882478.1:n.919+218del
XM_017026990.1:c.705+2036del	XP_016882479.1:n.705+2036del
NM_030662.4:c.919+218del MANE Select	NP_109587.1:n.919+218del