Canonical Allele Identifier: CA403382518

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094486-G-T
• MyVariant Identifiers: chr19:g.4094484G>T (hg19) ; chr19:g.4094486G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094486G>T , CM000681.2:g.4094486G>T	GRCh38
NC_000019.9:g.4094484G>T , CM000681.1:g.4094484G>T	GRCh37
NC_000019.8:g.4045484G>T	NCBI36
NG_007996.1:g.34643C>A , LRG_750:g.34643C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1498C>A
ENST00000688002.1:n.3210C>A
ENST00000688751.1:n.195C>A
ENST00000689792.1:n.963C>A
ENST00000262948.10:c.1059C>A MANE Select	ENSP00000262948.4:p.Asn353Lys
ENST00000262948.9:c.1059C>A	ENSP00000262948.3:p.Asn353Lys
ENST00000394867.8:c.768C>A	ENSP00000378336.1:p.Asn256Lys
ENST00000597263.5:n.244C>A
ENST00000599021.1:c.169C>A
ENST00000600584.5:n.2508C>A
ENST00000601786.5:n.1360C>A
NM_030662.3:c.1059C>A , LRG_750t1:c.1059C>A	NP_109587.1:p.Asn353Lys
XM_006722799.2:c.780C>A	XP_006722862.1:p.Asn260Lys
XM_011528133.1:c.489C>A	XP_011526435.1:p.Asn163Lys
NM_030662.4:c.1059C>A MANE Select	NP_109587.1:p.Asn353Lys