Canonical Allele Identifier: CA2766565147
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857447C>T , CM000667.2:g.56857447C>T GRCh38
NC_000005.9:g.56153274C>T , CM000667.1:g.56153274C>T GRCh37
NC_000005.8:g.56189031C>T NCBI36
NG_031884.1:g.47375C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.633+697C>T MANE Select ENSP00000382423.3:n.633+697C>T
ENST00000399503.3:c.633+697C>T ENSP00000382423.3:n.633+697C>T
NM_005921.1:c.633+697C>T NP_005912.1:n.633+697C>T
XM_005248519.3:c.255+697C>T XP_005248576.2:n.255+697C>T
XM_011543406.1:c.378+697C>T XP_011541708.1:n.378+697C>T
XM_011543407.1:c.633+697C>T XP_011541709.1:n.633+697C>T
XM_011543408.1:c.633+697C>T XP_011541710.1:n.633+697C>T
XM_017009484.1:c.222+697C>T XP_016864973.1:n.222+697C>T
XM_017009485.1:c.144+697C>T XP_016864974.1:n.144+697C>T
XR_001742068.2:n.664+697C>T
NM_005921.2:c.633+697C>T MANE Select NP_005912.1:n.633+697C>T