Canonical Allele Identifier: CA359802682

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155723A>T (hg19) ; chr5:g.56859896A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859896A>T , CM000667.2:g.56859896A>T	GRCh38
NC_000005.9:g.56155723A>T , CM000667.1:g.56155723A>T	GRCh37
NC_000005.8:g.56191480A>T	NCBI36
NG_031884.1:g.49824A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.815A>T MANE Select	ENSP00000382423.3:p.Lys272Ile
ENST00000399503.3:c.815A>T	ENSP00000382423.3:p.Lys272Ile
NM_005921.1:c.815A>T	NP_005912.1:p.Lys272Ile
XM_005248519.3:c.437A>T	XP_005248576.2:p.Lys146Ile
XM_011543406.1:c.560A>T	XP_011541708.1:p.Lys187Ile
XM_011543407.1:c.815A>T	XP_011541709.1:p.Lys272Ile
XM_011543408.1:c.815A>T	XP_011541710.1:p.Lys272Ile
XM_017009484.1:c.404A>T	XP_016864973.1:p.Lys135Ile
XM_017009485.1:c.326A>T	XP_016864974.1:p.Lys109Ile
XR_001742068.2:n.846A>T
NM_005921.2:c.815A>T MANE Select	NP_005912.1:p.Lys272Ile