Canonical Allele Identifier: CA444391664

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56859783-A-G
• MyVariant Identifiers: chr5:g.56155610A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859783A>G , CM000667.2:g.56859783A>G	GRCh38
NC_000005.9:g.56155610A>G , CM000667.1:g.56155610A>G	GRCh37
NC_000005.8:g.56191367A>G	NCBI36
NG_031884.1:g.49711A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.702A>G MANE Select	ENSP00000382423.3:p.Gly234=
ENST00000399503.3:c.702A>G	ENSP00000382423.3:p.Gly234=
NM_005921.1:c.702A>G	NP_005912.1:p.Gly234=
XM_005248519.3:c.324A>G	XP_005248576.2:p.Gly108=
XM_011543406.1:c.447A>G	XP_011541708.1:p.Gly149=
XM_011543407.1:c.702A>G	XP_011541709.1:p.Gly234=
XM_011543408.1:c.702A>G	XP_011541710.1:p.Gly234=
XM_017009484.1:c.291A>G	XP_016864973.1:p.Gly97=
XM_017009485.1:c.213A>G	XP_016864974.1:p.Gly71=
XR_001742068.2:n.733A>G
NM_005921.2:c.702A>G MANE Select	NP_005912.1:p.Gly234=