Canonical Allele Identifier: CA2766565213
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875398T>C , CM000667.2:g.56875398T>C GRCh38
NC_000005.9:g.56171225T>C , CM000667.1:g.56171225T>C GRCh37
NC_000005.8:g.56206982T>C NCBI36
NG_031884.1:g.65326T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1965+88T>C MANE Select ENSP00000382423.3:n.1965+88T>C
ENST00000399503.3:c.1965+88T>C ENSP00000382423.3:n.1965+88T>C
NM_005921.1:c.1965+88T>C NP_005912.1:n.1965+88T>C
XM_005248519.3:c.1587+88T>C XP_005248576.2:n.1587+88T>C
XM_011543406.1:c.1710+88T>C XP_011541708.1:n.1710+88T>C
XM_011543407.1:c.1686+2393T>C XP_011541709.1:n.1686+2393T>C
XM_011543408.1:c.1965+88T>C XP_011541710.1:n.1965+88T>C
XM_017009484.1:c.1554+88T>C XP_016864973.1:n.1554+88T>C
XM_017009485.1:c.1476+88T>C XP_016864974.1:n.1476+88T>C
XR_001742068.2:n.1996+88T>C
NM_005921.2:c.1965+88T>C MANE Select NP_005912.1:n.1965+88T>C