Canonical Allele Identifier: CA715112850

Gene: MAP2K5

Linked Data

• dbSNP Id: rs1162723981
• gnomAD v3: 15-67745252-G-T
• gnomAD v4: 15-67745252-G-T
• MyVariant Identifiers: chr15:g.68037590G>T (hg19) ; chr15:g.67745252G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67745252G>T , CM000677.2:g.67745252G>T	GRCh38
NC_000015.9:g.68037590G>T , CM000677.1:g.68037590G>T	GRCh37
NC_000015.8:g.65824644G>T	NCBI36
NG_029143.1:g.207570G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178640.10:c.1075-2979G>T MANE Select	ENSP00000178640.5:n.1075-2979G>T
ENST00000178640.9:c.1075-2979G>T	ENSP00000178640.5:n.1075-2979G>T
ENST00000340972.8:c.505-2979G>T	ENSP00000342101.4:n.505-2979G>T
ENST00000354498.9:c.967-2979G>T	ENSP00000346493.5:n.967-2979G>T
ENST00000395476.6:c.1045-2979G>T	ENSP00000378859.2:n.1045-2979G>T
ENST00000557869.2:c.52-3317G>T	ENSP00000483771.1:n.52-3317G>T
ENST00000558274.1:n.186-3317G>T
ENST00000558392.5:n.901-2979G>T
NM_001206804.1:c.967-2979G>T	NP_001193733.1:n.967-2979G>T
NM_002757.3:c.1045-2979G>T	NP_002748.1:n.1045-2979G>T
NM_145160.2:c.1075-2979G>T	NP_660143.1:n.1075-2979G>T
XM_011521784.1:c.1075-2979G>T	XP_011520086.1:n.1075-2979G>T
XM_011521785.1:c.1075-2979G>T	XP_011520087.1:n.1075-2979G>T
XM_011521786.1:c.1075-3317G>T	XP_011520088.1:n.1075-3317G>T
XM_024449988.1:c.844-2979G>T	XP_024305756.1:n.844-2979G>T
NM_145160.3:c.1075-2979G>T MANE Select	NP_660143.1:n.1075-2979G>T
NM_001206804.2:c.967-2979G>T	NP_001193733.1:n.967-2979G>T
NM_002757.4:c.1045-2979G>T	NP_002748.1:n.1045-2979G>T