Canonical Allele Identifier: CA403382542

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4094489T>G (hg19) ; chr19:g.4094491T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094491T>G , CM000681.2:g.4094491T>G	GRCh38
NC_000019.9:g.4094489T>G , CM000681.1:g.4094489T>G	GRCh37
NC_000019.8:g.4045489T>G	NCBI36
NG_007996.1:g.34638A>C , LRG_750:g.34638A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1493A>C
ENST00000688002.1:n.3205A>C
ENST00000688751.1:n.190A>C
ENST00000689792.1:n.958A>C
ENST00000262948.10:c.1054A>C MANE Select	ENSP00000262948.4:p.Lys352Gln
ENST00000262948.9:c.1054A>C	ENSP00000262948.3:p.Lys352Gln
ENST00000394867.8:c.763A>C	ENSP00000378336.1:p.Lys255Gln
ENST00000597263.5:n.239A>C
ENST00000599021.1:c.164A>C
ENST00000600584.5:n.2503A>C
ENST00000601786.5:n.1355A>C
NM_030662.3:c.1054A>C , LRG_750t1:c.1054A>C	NP_109587.1:p.Lys352Gln
XM_006722799.2:c.775A>C	XP_006722862.1:p.Lys259Gln
XM_011528133.1:c.484A>C	XP_011526435.1:p.Lys162Gln
NM_030662.4:c.1054A>C MANE Select	NP_109587.1:p.Lys352Gln