Canonical Allele Identifier: CA359803007
Community Standard Title: NM_005921.2(MAP3K1):c.963G>T (p.Gln321His)
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56864862G>T , CM000667.2:g.56864862G>T GRCh38
NC_000005.9:g.56160689G>T , CM000667.1:g.56160689G>T GRCh37
NC_000005.8:g.56196446G>T NCBI36
NG_031884.1:g.54790G>T

Transcript Alleles

HGVS Amino-acid Change
NM_005921.2:c.963G>T MANE Select NP_005912.1:p.Gln321His
ENST00000399503.4:c.963G>T MANE Select ENSP00000382423.3:p.Gln321His
NM_005921.1:c.963G>T NP_005912.1:p.Gln321His
ENST00000399503.3:c.963G>T ENSP00000382423.3:p.Gln321His
XM_005248519.3:c.585G>T XP_005248576.2:p.Gln195His
XM_011543406.1:c.708G>T XP_011541708.1:p.Gln236His
XM_011543407.1:c.963G>T XP_011541709.1:p.Gln321His
XM_011543408.1:c.963G>T XP_011541710.1:p.Gln321His
XM_017009484.1:c.552G>T XP_016864973.1:p.Gln184His
XM_017009485.1:c.474G>T XP_016864974.1:p.Gln158His
XR_001742068.2:n.994G>T