Canonical Allele Identifier: CA359787642

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945573
• MyVariant Identifiers: chr5:g.56178122A>G (hg19) ; chr5:g.56882295A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882295A>G , CM000667.2:g.56882295A>G	GRCh38
NC_000005.9:g.56178122A>G , CM000667.1:g.56178122A>G	GRCh37
NC_000005.8:g.56213879A>G	NCBI36
NG_031884.1:g.72223A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3095A>G MANE Select	ENSP00000382423.3:p.Asn1032Ser
ENST00000399503.3:c.3095A>G	ENSP00000382423.3:p.Asn1032Ser
NM_005921.1:c.3095A>G	NP_005912.1:p.Asn1032Ser
XM_005248519.3:c.2717A>G	XP_005248576.2:p.Asn906Ser
XM_011543406.1:c.2840A>G	XP_011541708.1:p.Asn947Ser
XM_011543407.1:c.2816A>G	XP_011541709.1:p.Asn939Ser
XM_011543408.1:c.3095A>G	XP_011541710.1:p.Asn1032Ser
XM_017009484.1:c.2684A>G	XP_016864973.1:p.Asn895Ser
XM_017009485.1:c.2606A>G	XP_016864974.1:p.Asn869Ser
XR_001742068.2:n.3126A>G
NM_005921.2:c.3095A>G MANE Select	NP_005912.1:p.Asn1032Ser