Canonical Allele Identifier: CA403380681

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040845921
• MyVariant Identifiers: chr19:g.4090613T>C (hg19) ; chr19:g.4090615T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090615T>C , CM000681.2:g.4090615T>C	GRCh38
NC_000019.9:g.4090613T>C , CM000681.1:g.4090613T>C	GRCh37
NC_000019.8:g.4041613T>C	NCBI36
NG_007996.1:g.38514A>G , LRG_750:g.38514A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1625A>G
ENST00000688002.1:n.3337A>G
ENST00000688751.1:n.322A>G
ENST00000689792.1:n.1090A>G
ENST00000262948.10:c.1186A>G MANE Select	ENSP00000262948.4:p.Thr396Ala
ENST00000262948.9:c.1186A>G	ENSP00000262948.3:p.Thr396Ala
ENST00000394867.8:c.895A>G	ENSP00000378336.1:p.Thr299Ala
ENST00000597263.5:n.371A>G
ENST00000599021.1:c.296A>G
ENST00000600584.5:n.2635A>G
ENST00000601786.5:n.1487A>G
NM_030662.3:c.1186A>G , LRG_750t1:c.1186A>G	NP_109587.1:p.Thr396Ala
XM_006722799.2:c.907A>G	XP_006722862.1:p.Thr303Ala
XM_011528133.1:c.616A>G	XP_011526435.1:p.Thr206Ala
NM_030662.4:c.1186A>G MANE Select	NP_109587.1:p.Thr396Ala