Canonical Allele Identifier: CA403380594

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4090600A>C (hg19) ; chr19:g.4090602A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090602A>C , CM000681.2:g.4090602A>C	GRCh38
NC_000019.9:g.4090600A>C , CM000681.1:g.4090600A>C	GRCh37
NC_000019.8:g.4041600A>C	NCBI36
NG_007996.1:g.38527T>G , LRG_750:g.38527T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1638T>G
ENST00000688002.1:n.3350T>G
ENST00000688751.1:n.335T>G
ENST00000689792.1:n.1103T>G
ENST00000262948.10:c.1199T>G MANE Select	ENSP00000262948.4:p.Val400Gly
ENST00000262948.9:c.1199T>G	ENSP00000262948.3:p.Val400Gly
ENST00000394867.8:c.908T>G	ENSP00000378336.1:p.Val303Gly
ENST00000597263.5:n.384T>G
ENST00000599021.1:c.309T>G
ENST00000600584.5:n.2648T>G
ENST00000601786.5:n.1500T>G
NM_030662.3:c.1199T>G , LRG_750t1:c.1199T>G	NP_109587.1:p.Val400Gly
XM_006722799.2:c.920T>G	XP_006722862.1:p.Val307Gly
XM_011528133.1:c.629T>G	XP_011526435.1:p.Val210Gly
NM_030662.4:c.1199T>G MANE Select	NP_109587.1:p.Val400Gly