Canonical Allele Identifier: CA14084698
Gene: MAP2K5 HGNC NCBI

Linked Data

dbSNP Id: rs884202
gnomAD v2: 15-68054388-G-A
gnomAD v3: 15-67762050-G-A
gnomAD v4: 15-67762050-G-A
MyVariant Identifiers: chr15:g.68054388G>A (hg19) chr15:g.67762050G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67762050G>A , CM000677.2:g.67762050G>A GRCh38
NC_000015.9:g.68054388G>A , CM000677.1:g.68054388G>A GRCh37
NC_000015.8:g.65841442G>A NCBI36
NG_029143.1:g.224368G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000178640.10:c.1135-7552G>A MANE Select ENSP00000178640.5:n.1135-7552G>A
ENST00000178640.9:c.1135-7552G>A ENSP00000178640.5:n.1135-7552G>A
ENST00000340972.8:c.565-7552G>A ENSP00000342101.4:n.565-7552G>A
ENST00000354498.9:c.1027-7552G>A ENSP00000346493.5:n.1027-7552G>A
ENST00000395476.6:c.1105-7552G>A ENSP00000378859.2:n.1105-7552G>A
ENST00000557869.2:c.85-7552G>A ENSP00000483771.1:n.85-7552G>A
ENST00000558021.1:n.235-7552G>A
ENST00000558274.1:n.219-7552G>A
ENST00000558392.5:n.961-7552G>A
NM_001206804.1:c.1027-7552G>A NP_001193733.1:n.1027-7552G>A
NM_002757.3:c.1105-7552G>A NP_002748.1:n.1105-7552G>A
NM_145160.2:c.1135-7552G>A NP_660143.1:n.1135-7552G>A
XM_011521784.1:c.1135-4672G>A XP_011520086.1:n.1135-4672G>A
XM_011521785.1:c.1135-4672G>A XP_011520087.1:n.1135-4672G>A
XM_011521786.1:c.1108-7552G>A XP_011520088.1:n.1108-7552G>A
XM_024449988.1:c.904-7552G>A XP_024305756.1:n.904-7552G>A
NM_145160.3:c.1135-7552G>A MANE Select NP_660143.1:n.1135-7552G>A
NM_001206804.2:c.1027-7552G>A NP_001193733.1:n.1027-7552G>A
NM_002757.4:c.1105-7552G>A NP_002748.1:n.1105-7552G>A
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