Canonical Allele Identifier: CA444399052
Gene: MAP3K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.56177436G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881609G>A , CM000667.2:g.56881609G>A GRCh38
NC_000005.9:g.56177436G>A , CM000667.1:g.56177436G>A GRCh37
NC_000005.8:g.56213193G>A NCBI36
NG_031884.1:g.71537G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2409G>A MANE Select ENSP00000382423.3:p.Gln803=
ENST00000399503.3:c.2409G>A ENSP00000382423.3:p.Gln803=
NM_005921.1:c.2409G>A NP_005912.1:p.Gln803=
XM_005248519.3:c.2031G>A XP_005248576.2:p.Gln677=
XM_011543406.1:c.2154G>A XP_011541708.1:p.Gln718=
XM_011543407.1:c.2130G>A XP_011541709.1:p.Gln710=
XM_011543408.1:c.2409G>A XP_011541710.1:p.Gln803=
XM_017009484.1:c.1998G>A XP_016864973.1:p.Gln666=
XM_017009485.1:c.1920G>A XP_016864974.1:p.Gln640=
XR_001742068.2:n.2440G>A
NM_005921.2:c.2409G>A MANE Select NP_005912.1:p.Gln803=