Canonical Allele Identifier: CA304447632

Gene: MAP2K2

Linked Data

• dbSNP Id: rs778976972
• MyVariant Identifiers: chr19:g.4095624_4095625del (hg19) ; chr19:g.4095626_4095627del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095629_4095630del , CM000681.2:g.4095629_4095630del	GRCh38
NC_000019.9:g.4095627_4095628del , CM000681.1:g.4095627_4095628del	GRCh37
NC_000019.8:g.4046627_4046628del	NCBI36
NG_007996.1:g.33502_33503del , LRG_750:g.33502_33503del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-178_1424-177del
ENST00000688002.1:n.3136-178_3136-177del
ENST00000688751.1:n.121-178_121-177del
ENST00000689792.1:n.889-178_889-177del
ENST00000262948.10:c.985-178_985-177del MANE Select	ENSP00000262948.4:n.985-178_985-177del
ENST00000262948.9:c.985-178_985-177del	ENSP00000262948.3:n.985-178_985-177del
ENST00000394867.8:c.694-178_694-177del	ENSP00000378336.1:n.694-178_694-177del
ENST00000595715.1:n.800-178_800-177del
ENST00000597263.5:n.170-178_170-177del
ENST00000599021.1:c.95-178_95-177del
ENST00000600584.5:n.1545-178_1545-177del
ENST00000601786.5:n.1286-178_1286-177del
NM_030662.3:c.985-178_985-177del , LRG_750t1:c.985-178_985-177del	NP_109587.1:n.985-178_985-177del
XM_006722799.2:c.706-178_706-177del	XP_006722862.1:n.706-178_706-177del
XM_011528133.1:c.415-178_415-177del	XP_011526435.1:n.415-178_415-177del
XM_017026989.1:c.985-178_985-177del	XP_016882478.1:n.985-178_985-177del
XM_017026990.1:c.706-178_706-177del	XP_016882479.1:n.706-178_706-177del
NM_030662.4:c.985-178_985-177del MANE Select	NP_109587.1:n.985-178_985-177del