Canonical Allele Identifier: CA882243688

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1190146307
• MyVariant Identifiers: chr19:g.4099155_4099165del (hg19) ; chr19:g.4099157_4099167del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099158_4099168del , CM000681.2:g.4099158_4099168del	GRCh38
NC_000019.9:g.4099156_4099166del , CM000681.1:g.4099156_4099166del	GRCh37
NC_000019.8:g.4050156_4050166del	NCBI36
NG_007996.1:g.29962_29972del , LRG_750:g.29962_29972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+34_1358+44del
ENST00000687128.1:n.1392_1402del
ENST00000688002.1:n.1247_1257del
ENST00000689792.1:n.823+34_823+44del
ENST00000262948.10:c.919+34_919+44del MANE Select	ENSP00000262948.4:n.919+34_919+44del
ENST00000262948.9:c.919+34_919+44del	ENSP00000262948.3:n.919+34_919+44del
ENST00000394867.8:c.628+34_628+44del	ENSP00000378336.1:n.628+34_628+44del
ENST00000595715.1:n.734+34_734+44del
ENST00000597263.5:n.169+1852_169+1862del
ENST00000599021.1:c.30-1824_30-1814del
ENST00000600584.5:n.1479+34_1479+44del
ENST00000601786.5:n.1220+34_1220+44del
NM_030662.3:c.919+34_919+44del , LRG_750t1:c.919+34_919+44del	NP_109587.1:n.919+34_919+44del
XM_006722799.2:c.705+1852_705+1862del	XP_006722862.1:n.705+1852_705+1862del
XM_011528133.1:c.349+34_349+44del	XP_011526435.1:n.349+34_349+44del
XM_017026989.1:c.919+34_919+44del	XP_016882478.1:n.919+34_919+44del
XM_017026990.1:c.705+1852_705+1862del	XP_016882479.1:n.705+1852_705+1862del
NM_030662.4:c.919+34_919+44del MANE Select	NP_109587.1:n.919+34_919+44del