Canonical Allele Identifier: CA1548139575
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882385C= , CM000667.2:g.56882385C= GRCh38
NC_000005.9:g.56178212C= , CM000667.1:g.56178212C= GRCh37
NC_000005.8:g.56213969C= NCBI36
NG_031884.1:g.72313C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3185C= MANE Select ENSP00000382423.3:p.Pro1062=
ENST00000399503.3:c.3185C= ENSP00000382423.3:p.Pro1062=
NM_005921.1:c.3185C= NP_005912.1:p.Pro1062=
XM_005248519.3:c.2807C= XP_005248576.2:p.Pro936=
XM_011543406.1:c.2930C= XP_011541708.1:p.Pro977=
XM_011543407.1:c.2906C= XP_011541709.1:p.Pro969=
XM_011543408.1:c.3185C= XP_011541710.1:p.Pro1062=
XM_017009484.1:c.2774C= XP_016864973.1:p.Pro925=
XM_017009485.1:c.2696C= XP_016864974.1:p.Pro899=
XR_001742068.2:n.3216C=
NM_005921.2:c.3185C= MANE Select NP_005912.1:p.Pro1062=