Canonical Allele Identifier: CA359787505

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178057T>G (hg19) ; chr5:g.56882230T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882230T>G , CM000667.2:g.56882230T>G	GRCh38
NC_000005.9:g.56178057T>G , CM000667.1:g.56178057T>G	GRCh37
NC_000005.8:g.56213814T>G	NCBI36
NG_031884.1:g.72158T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3030T>G MANE Select	ENSP00000382423.3:p.Ile1010Met
ENST00000399503.3:c.3030T>G	ENSP00000382423.3:p.Ile1010Met
NM_005921.1:c.3030T>G	NP_005912.1:p.Ile1010Met
XM_005248519.3:c.2652T>G	XP_005248576.2:p.Ile884Met
XM_011543406.1:c.2775T>G	XP_011541708.1:p.Ile925Met
XM_011543407.1:c.2751T>G	XP_011541709.1:p.Ile917Met
XM_011543408.1:c.3030T>G	XP_011541710.1:p.Ile1010Met
XM_017009484.1:c.2619T>G	XP_016864973.1:p.Ile873Met
XM_017009485.1:c.2541T>G	XP_016864974.1:p.Ile847Met
XR_001742068.2:n.3061T>G
NM_005921.2:c.3030T>G MANE Select	NP_005912.1:p.Ile1010Met