Canonical Allele Identifier: CA403380754
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090625G>C (hg19) chr19:g.4090627G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090627G>C , CM000681.2:g.4090627G>C GRCh38
NC_000019.9:g.4090625G>C , CM000681.1:g.4090625G>C GRCh37
NC_000019.8:g.4041625G>C NCBI36
NG_007996.1:g.38502C>G , LRG_750:g.38502C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1613C>G
ENST00000688002.1:n.3325C>G
ENST00000688751.1:n.310C>G
ENST00000689792.1:n.1078C>G
ENST00000262948.10:c.1174C>G MANE Select ENSP00000262948.4:p.Pro392Ala
ENST00000262948.9:c.1174C>G ENSP00000262948.3:p.Pro392Ala
ENST00000394867.8:c.883C>G ENSP00000378336.1:p.Pro295Ala
ENST00000597263.5:n.359C>G
ENST00000599021.1:c.284C>G
ENST00000600584.5:n.2623C>G
ENST00000601786.5:n.1475C>G
NM_030662.3:c.1174C>G , LRG_750t1:c.1174C>G NP_109587.1:p.Pro392Ala
XM_006722799.2:c.895C>G XP_006722862.1:p.Pro299Ala
XM_011528133.1:c.604C>G XP_011526435.1:p.Pro202Ala
NM_030662.4:c.1174C>G MANE Select NP_109587.1:p.Pro392Ala
Search 100 bp 5'
Search 100 bp 3'