Canonical Allele Identifier: CA359786028

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177572T>A (hg19) ; chr5:g.56881745T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881745T>A , CM000667.2:g.56881745T>A	GRCh38
NC_000005.9:g.56177572T>A , CM000667.1:g.56177572T>A	GRCh37
NC_000005.8:g.56213329T>A	NCBI36
NG_031884.1:g.71673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2545T>A MANE Select	ENSP00000382423.3:p.Phe849Ile
ENST00000399503.3:c.2545T>A	ENSP00000382423.3:p.Phe849Ile
NM_005921.1:c.2545T>A	NP_005912.1:p.Phe849Ile
XM_005248519.3:c.2167T>A	XP_005248576.2:p.Phe723Ile
XM_011543406.1:c.2290T>A	XP_011541708.1:p.Phe764Ile
XM_011543407.1:c.2266T>A	XP_011541709.1:p.Phe756Ile
XM_011543408.1:c.2545T>A	XP_011541710.1:p.Phe849Ile
XM_017009484.1:c.2134T>A	XP_016864973.1:p.Phe712Ile
XM_017009485.1:c.2056T>A	XP_016864974.1:p.Phe686Ile
XR_001742068.2:n.2576T>A
NM_005921.2:c.2545T>A MANE Select	NP_005912.1:p.Phe849Ile