Canonical Allele Identifier: CA119080202
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs372668075

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882394C>G , CM000667.2:g.56882394C>G GRCh38
NC_000005.9:g.56178221C>G , CM000667.1:g.56178221C>G GRCh37
NC_000005.8:g.56213978C>G NCBI36
NG_031884.1:g.72322C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3194C>G MANE Select ENSP00000382423.3:p.Pro1065Arg
ENST00000399503.3:c.3194C>G ENSP00000382423.3:p.Pro1065Arg
NM_005921.1:c.3194C>G NP_005912.1:p.Pro1065Arg
XM_005248519.3:c.2816C>G XP_005248576.2:p.Pro939Arg
XM_011543406.1:c.2939C>G XP_011541708.1:p.Pro980Arg
XM_011543407.1:c.2915C>G XP_011541709.1:p.Pro972Arg
XM_011543408.1:c.3194C>G XP_011541710.1:p.Pro1065Arg
XM_017009484.1:c.2783C>G XP_016864973.1:p.Pro928Arg
XM_017009485.1:c.2705C>G XP_016864974.1:p.Pro902Arg
XR_001742068.2:n.3225C>G
NM_005921.2:c.3194C>G MANE Select NP_005912.1:p.Pro1065Arg