Canonical Allele Identifier: CA359787795
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111946183

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882364G>A , CM000667.2:g.56882364G>A GRCh38
NC_000005.9:g.56178191G>A , CM000667.1:g.56178191G>A GRCh37
NC_000005.8:g.56213948G>A NCBI36
NG_031884.1:g.72292G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3164G>A MANE Select ENSP00000382423.3:p.Ser1055Asn
ENST00000399503.3:c.3164G>A ENSP00000382423.3:p.Ser1055Asn
NM_005921.1:c.3164G>A NP_005912.1:p.Ser1055Asn
XM_005248519.3:c.2786G>A XP_005248576.2:p.Ser929Asn
XM_011543406.1:c.2909G>A XP_011541708.1:p.Ser970Asn
XM_011543407.1:c.2885G>A XP_011541709.1:p.Ser962Asn
XM_011543408.1:c.3164G>A XP_011541710.1:p.Ser1055Asn
XM_017009484.1:c.2753G>A XP_016864973.1:p.Ser918Asn
XM_017009485.1:c.2675G>A XP_016864974.1:p.Ser892Asn
XR_001742068.2:n.3195G>A
NM_005921.2:c.3164G>A MANE Select NP_005912.1:p.Ser1055Asn