Canonical Allele Identifier: CA359787674
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111945689

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882308C>G , CM000667.2:g.56882308C>G GRCh38
NC_000005.9:g.56178135C>G , CM000667.1:g.56178135C>G GRCh37
NC_000005.8:g.56213892C>G NCBI36
NG_031884.1:g.72236C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3108C>G MANE Select ENSP00000382423.3:p.Asn1036Lys
ENST00000399503.3:c.3108C>G ENSP00000382423.3:p.Asn1036Lys
NM_005921.1:c.3108C>G NP_005912.1:p.Asn1036Lys
XM_005248519.3:c.2730C>G XP_005248576.2:p.Asn910Lys
XM_011543406.1:c.2853C>G XP_011541708.1:p.Asn951Lys
XM_011543407.1:c.2829C>G XP_011541709.1:p.Asn943Lys
XM_011543408.1:c.3108C>G XP_011541710.1:p.Asn1036Lys
XM_017009484.1:c.2697C>G XP_016864973.1:p.Asn899Lys
XM_017009485.1:c.2619C>G XP_016864974.1:p.Asn873Lys
XR_001742068.2:n.3139C>G
NM_005921.2:c.3108C>G MANE Select NP_005912.1:p.Asn1036Lys