Canonical Allele Identifier: CA403380585

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4090597C>G (hg19) ; chr19:g.4090599C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090599C>G , CM000681.2:g.4090599C>G	GRCh38
NC_000019.9:g.4090597C>G , CM000681.1:g.4090597C>G	GRCh37
NC_000019.8:g.4041597C>G	NCBI36
NG_007996.1:g.38530G>C , LRG_750:g.38530G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1641G>C
ENST00000688002.1:n.3353G>C
ENST00000688751.1:n.338G>C
ENST00000689792.1:n.1106G>C
ENST00000262948.10:c.1202G>C MANE Select	ENSP00000262948.4:p.Ter401Ser
ENST00000262948.9:c.1202G>C	ENSP00000262948.3:p.Ter401Ser
ENST00000394867.8:c.911G>C	ENSP00000378336.1:p.Ter304Ser
ENST00000597263.5:n.387G>C
ENST00000599021.1:c.312G>C
ENST00000600584.5:n.2651G>C
ENST00000601786.5:n.1503G>C
NM_030662.3:c.1202G>C , LRG_750t1:c.1202G>C	NP_109587.1:p.Ter401Ser
XM_006722799.2:c.923G>C	XP_006722862.1:p.Ter308Ser
XM_011528133.1:c.632G>C	XP_011526435.1:p.Ter211Ser
NM_030662.4:c.1202G>C MANE Select	NP_109587.1:p.Ter401Ser