Canonical Allele Identifier: CA3273040
Community Standard Title: NM_005921.2(MAP3K1):c.2668C>T (p.Pro890Ser)
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881868C>T , CM000667.2:g.56881868C>T GRCh38
NC_000005.9:g.56177695C>T , CM000667.1:g.56177695C>T GRCh37
NC_000005.8:g.56213452C>T NCBI36
NG_031884.1:g.71796C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005921.2:c.2668C>T MANE Select NP_005912.1:p.Pro890Ser
ENST00000399503.4:c.2668C>T MANE Select ENSP00000382423.3:p.Pro890Ser
NM_005921.1:c.2668C>T NP_005912.1:p.Pro890Ser
ENST00000399503.3:c.2668C>T ENSP00000382423.3:p.Pro890Ser
XM_005248519.3:c.2290C>T XP_005248576.2:p.Pro764Ser
XM_011543406.1:c.2413C>T XP_011541708.1:p.Pro805Ser
XM_011543407.1:c.2389C>T XP_011541709.1:p.Pro797Ser
XM_011543408.1:c.2668C>T XP_011541710.1:p.Pro890Ser
XM_017009484.1:c.2257C>T XP_016864973.1:p.Pro753Ser
XM_017009485.1:c.2179C>T XP_016864974.1:p.Pro727Ser
XR_001742068.2:n.2699C>T