Canonical Allele Identifier: CA403383430

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4095436C>G (hg19) ; chr19:g.4095438C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095438C>G , CM000681.2:g.4095438C>G	GRCh38
NC_000019.9:g.4095436C>G , CM000681.1:g.4095436C>G	GRCh37
NC_000019.8:g.4046436C>G	NCBI36
NG_007996.1:g.33691G>C , LRG_750:g.33691G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1435G>C
ENST00000688002.1:n.3147G>C
ENST00000688751.1:n.132G>C
ENST00000689792.1:n.900G>C
ENST00000262948.10:c.996G>C MANE Select	ENSP00000262948.4:p.Lys332Asn
ENST00000262948.9:c.996G>C	ENSP00000262948.3:p.Lys332Asn
ENST00000394867.8:c.705G>C	ENSP00000378336.1:p.Lys235Asn
ENST00000595715.1:n.811G>C
ENST00000597263.5:n.181G>C
ENST00000599021.1:c.106G>C
ENST00000600584.5:n.1556G>C
ENST00000601786.5:n.1297G>C
NM_030662.3:c.996G>C , LRG_750t1:c.996G>C	NP_109587.1:p.Lys332Asn
XM_006722799.2:c.717G>C	XP_006722862.1:p.Lys239Asn
XM_011528133.1:c.426G>C	XP_011526435.1:p.Lys142Asn
XM_017026989.1:c.996G>C	XP_016882478.1:p.Lys332Asn
XM_017026990.1:c.717G>C	XP_016882479.1:p.Lys239Asn
NM_030662.4:c.996G>C MANE Select	NP_109587.1:p.Lys332Asn