Canonical Allele Identifier: CA14084701

Gene: MAP2K5

Linked Data

• dbSNP Id: rs3784709
• gnomAD v2: 15-68072275-C-T
• gnomAD v3: 15-67779937-C-T
• gnomAD v4: 15-67779937-C-T
• MyVariant Identifiers: chr15:g.68072275C>T (hg19) ; chr15:g.67779937C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67779937C>T , CM000677.2:g.67779937C>T	GRCh38
NC_000015.9:g.68072275C>T , CM000677.1:g.68072275C>T	GRCh37
NC_000015.8:g.65859329C>T	NCBI36
NG_029143.1:g.242255C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000178640.10:c.1242+7185C>T MANE Select	ENSP00000178640.5:n.1242+7185C>T
ENST00000178640.9:c.1242+7185C>T	ENSP00000178640.5:n.1242+7185C>T
ENST00000340972.8:c.672+7185C>T	ENSP00000342101.4:n.672+7185C>T
ENST00000354498.9:c.1134+7185C>T	ENSP00000346493.5:n.1134+7185C>T
ENST00000395476.6:c.1212+7185C>T	ENSP00000378859.2:n.1212+7185C>T
ENST00000558274.1:n.326+7185C>T
ENST00000558392.5:n.1068+7185C>T
NM_001206804.1:c.1134+7185C>T	NP_001193733.1:n.1134+7185C>T
NM_002757.3:c.1212+7185C>T	NP_002748.1:n.1212+7185C>T
NM_145160.2:c.1242+7185C>T	NP_660143.1:n.1242+7185C>T
XM_011521784.1:c.1287+7185C>T	XP_011520086.1:n.1287+7185C>T
XM_011521786.1:c.1215+7185C>T	XP_011520088.1:n.1215+7185C>T
XM_024449988.1:c.1011+7185C>T	XP_024305756.1:n.1011+7185C>T
NM_145160.3:c.1242+7185C>T MANE Select	NP_660143.1:n.1242+7185C>T
NM_001206804.2:c.1134+7185C>T	NP_001193733.1:n.1134+7185C>T
NM_002757.4:c.1212+7185C>T	NP_002748.1:n.1212+7185C>T