Canonical Allele Identifier: CA359787081
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882108T>C , CM000667.2:g.56882108T>C GRCh38
NC_000005.9:g.56177935T>C , CM000667.1:g.56177935T>C GRCh37
NC_000005.8:g.56213692T>C NCBI36
NG_031884.1:g.72036T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2908T>C MANE Select ENSP00000382423.3:p.Ser970Pro
ENST00000399503.3:c.2908T>C ENSP00000382423.3:p.Ser970Pro
NM_005921.1:c.2908T>C NP_005912.1:p.Ser970Pro
XM_005248519.3:c.2530T>C XP_005248576.2:p.Ser844Pro
XM_011543406.1:c.2653T>C XP_011541708.1:p.Ser885Pro
XM_011543407.1:c.2629T>C XP_011541709.1:p.Ser877Pro
XM_011543408.1:c.2908T>C XP_011541710.1:p.Ser970Pro
XM_017009484.1:c.2497T>C XP_016864973.1:p.Ser833Pro
XM_017009485.1:c.2419T>C XP_016864974.1:p.Ser807Pro
XR_001742068.2:n.2939T>C
NM_005921.2:c.2908T>C MANE Select NP_005912.1:p.Ser970Pro