Canonical Allele Identifier: CA359787041

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177926T>A (hg19) ; chr5:g.56882099T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882099T>A , CM000667.2:g.56882099T>A	GRCh38
NC_000005.9:g.56177926T>A , CM000667.1:g.56177926T>A	GRCh37
NC_000005.8:g.56213683T>A	NCBI36
NG_031884.1:g.72027T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2899T>A MANE Select	ENSP00000382423.3:p.Leu967Met
ENST00000399503.3:c.2899T>A	ENSP00000382423.3:p.Leu967Met
NM_005921.1:c.2899T>A	NP_005912.1:p.Leu967Met
XM_005248519.3:c.2521T>A	XP_005248576.2:p.Leu841Met
XM_011543406.1:c.2644T>A	XP_011541708.1:p.Leu882Met
XM_011543407.1:c.2620T>A	XP_011541709.1:p.Leu874Met
XM_011543408.1:c.2899T>A	XP_011541710.1:p.Leu967Met
XM_017009484.1:c.2488T>A	XP_016864973.1:p.Leu830Met
XM_017009485.1:c.2410T>A	XP_016864974.1:p.Leu804Met
XR_001742068.2:n.2930T>A
NM_005921.2:c.2899T>A MANE Select	NP_005912.1:p.Leu967Met