Canonical Allele Identifier: CA359787645

Gene: MAP3K1

Linked Data

• dbSNP Id: rs761930383
• gnomAD v4: 5-56882296-C-G
• MyVariant Identifiers: chr5:g.56178123C>G (hg19) ; chr5:g.56882296C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882296C>G , CM000667.2:g.56882296C>G	GRCh38
NC_000005.9:g.56178123C>G , CM000667.1:g.56178123C>G	GRCh37
NC_000005.8:g.56213880C>G	NCBI36
NG_031884.1:g.72224C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3096C>G MANE Select	ENSP00000382423.3:p.Asn1032Lys
ENST00000399503.3:c.3096C>G	ENSP00000382423.3:p.Asn1032Lys
NM_005921.1:c.3096C>G	NP_005912.1:p.Asn1032Lys
XM_005248519.3:c.2718C>G	XP_005248576.2:p.Asn906Lys
XM_011543406.1:c.2841C>G	XP_011541708.1:p.Asn947Lys
XM_011543407.1:c.2817C>G	XP_011541709.1:p.Asn939Lys
XM_011543408.1:c.3096C>G	XP_011541710.1:p.Asn1032Lys
XM_017009484.1:c.2685C>G	XP_016864973.1:p.Asn895Lys
XM_017009485.1:c.2607C>G	XP_016864974.1:p.Asn869Lys
XR_001742068.2:n.3127C>G
NM_005921.2:c.3096C>G MANE Select	NP_005912.1:p.Asn1032Lys