Canonical Allele Identifier: CA444398906

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170932_56170933insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875107dup , CM000667.2:g.56875107dup	GRCh38
NC_000005.9:g.56170934dup , CM000667.1:g.56170934dup	GRCh37
NC_000005.8:g.56206691dup	NCBI36
NG_031884.1:g.65035dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1762dup MANE Select	ENSP00000382423.3:p.Ser588PhefsTer3
ENST00000399503.3:c.1762dup	ENSP00000382423.3:p.Ser588PhefsTer3
NM_005921.1:c.1762dup	NP_005912.1:p.Ser588PhefsTer3
XM_005248519.3:c.1384dup	XP_005248576.2:p.Ser462PhefsTer3
XM_011543406.1:c.1507dup	XP_011541708.1:p.Ser503PhefsTer3
XM_011543407.1:c.1686+2102dup	XP_011541709.1:n.1686+2102dup
XM_011543408.1:c.1762dup	XP_011541710.1:p.Ser588PhefsTer3
XM_017009484.1:c.1351dup	XP_016864973.1:p.Ser451PhefsTer3
XM_017009485.1:c.1273dup	XP_016864974.1:p.Ser425PhefsTer3
XR_001742068.2:n.1793dup
NM_005921.2:c.1762dup MANE Select	NP_005912.1:p.Ser588PhefsTer3