Canonical Allele Identifier: CA359782517
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56878999T>C , CM000667.2:g.56878999T>C GRCh38
NC_000005.9:g.56174826T>C , CM000667.1:g.56174826T>C GRCh37
NC_000005.8:g.56210583T>C NCBI36
NG_031884.1:g.68927T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1985T>C MANE Select ENSP00000382423.3:p.Leu662Pro
ENST00000399503.3:c.1985T>C ENSP00000382423.3:p.Leu662Pro
NM_005921.1:c.1985T>C NP_005912.1:p.Leu662Pro
XM_005248519.3:c.1607T>C XP_005248576.2:p.Leu536Pro
XM_011543406.1:c.1730T>C XP_011541708.1:p.Leu577Pro
XM_011543407.1:c.1706T>C XP_011541709.1:p.Leu569Pro
XM_011543408.1:c.1985T>C XP_011541710.1:p.Leu662Pro
XM_017009484.1:c.1574T>C XP_016864973.1:p.Leu525Pro
XM_017009485.1:c.1496T>C XP_016864974.1:p.Leu499Pro
XR_001742068.2:n.2016T>C
NM_005921.2:c.1985T>C MANE Select NP_005912.1:p.Leu662Pro