Canonical Allele Identifier: CA504984451

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4094481T>G (hg19)

Genomic Alleles

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

Transcript Alleles

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