Canonical Allele Identifier: CA2766565308
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56860010G>C , CM000667.2:g.56860010G>C GRCh38
NC_000005.9:g.56155837G>C , CM000667.1:g.56155837G>C GRCh37
NC_000005.8:g.56191594G>C NCBI36
NG_031884.1:g.49938G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+95G>C MANE Select ENSP00000382423.3:n.834+95G>C
ENST00000399503.3:c.834+95G>C ENSP00000382423.3:n.834+95G>C
NM_005921.1:c.834+95G>C NP_005912.1:n.834+95G>C
XM_005248519.3:c.456+95G>C XP_005248576.2:n.456+95G>C
XM_011543406.1:c.579+95G>C XP_011541708.1:n.579+95G>C
XM_011543407.1:c.834+95G>C XP_011541709.1:n.834+95G>C
XM_011543408.1:c.834+95G>C XP_011541710.1:n.834+95G>C
XM_017009484.1:c.423+95G>C XP_016864973.1:n.423+95G>C
XM_017009485.1:c.345+95G>C XP_016864974.1:n.345+95G>C
XR_001742068.2:n.865+95G>C
NM_005921.2:c.834+95G>C MANE Select NP_005912.1:n.834+95G>C