Canonical Allele Identifier: CA359785768

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177452C>A (hg19) ; chr5:g.56881625C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881625C>A , CM000667.2:g.56881625C>A	GRCh38
NC_000005.9:g.56177452C>A , CM000667.1:g.56177452C>A	GRCh37
NC_000005.8:g.56213209C>A	NCBI36
NG_031884.1:g.71553C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2425C>A MANE Select	ENSP00000382423.3:p.His809Asn
ENST00000399503.3:c.2425C>A	ENSP00000382423.3:p.His809Asn
NM_005921.1:c.2425C>A	NP_005912.1:p.His809Asn
XM_005248519.3:c.2047C>A	XP_005248576.2:p.His683Asn
XM_011543406.1:c.2170C>A	XP_011541708.1:p.His724Asn
XM_011543407.1:c.2146C>A	XP_011541709.1:p.His716Asn
XM_011543408.1:c.2425C>A	XP_011541710.1:p.His809Asn
XM_017009484.1:c.2014C>A	XP_016864973.1:p.His672Asn
XM_017009485.1:c.1936C>A	XP_016864974.1:p.His646Asn
XR_001742068.2:n.2456C>A
NM_005921.2:c.2425C>A MANE Select	NP_005912.1:p.His809Asn