Canonical Allele Identifier: CA504984450

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094483-T-C
• MyVariant Identifiers: chr19:g.4094481T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094483T>C , CM000681.2:g.4094483T>C	GRCh38
NC_000019.9:g.4094481T>C , CM000681.1:g.4094481T>C	GRCh37
NC_000019.8:g.4045481T>C	NCBI36
NG_007996.1:g.34646A>G , LRG_750:g.34646A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1501A>G
ENST00000688002.1:n.3213A>G
ENST00000688751.1:n.198A>G
ENST00000689792.1:n.966A>G
ENST00000262948.10:c.1062A>G MANE Select	ENSP00000262948.4:p.Pro354=
ENST00000262948.9:c.1062A>G	ENSP00000262948.3:p.Pro354=
ENST00000394867.8:c.771A>G	ENSP00000378336.1:p.Pro257=
ENST00000597263.5:n.247A>G
ENST00000599021.1:c.172A>G
ENST00000600584.5:n.2511A>G
ENST00000601786.5:n.1363A>G
NM_030662.3:c.1062A>G , LRG_750t1:c.1062A>G	NP_109587.1:p.Pro354=
XM_006722799.2:c.783A>G	XP_006722862.1:p.Pro261=
XM_011528133.1:c.492A>G	XP_011526435.1:p.Pro164=
NM_030662.4:c.1062A>G MANE Select	NP_109587.1:p.Pro354=