Canonical Allele Identifier: CA359787640

Gene: MAP3K1

Linked Data

• dbSNP Id: rs774670651
• MyVariant Identifiers: chr5:g.56178121A>T (hg19) ; chr5:g.56882294A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882294A>T , CM000667.2:g.56882294A>T	GRCh38
NC_000005.9:g.56178121A>T , CM000667.1:g.56178121A>T	GRCh37
NC_000005.8:g.56213878A>T	NCBI36
NG_031884.1:g.72222A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3094A>T MANE Select	ENSP00000382423.3:p.Asn1032Tyr
ENST00000399503.3:c.3094A>T	ENSP00000382423.3:p.Asn1032Tyr
NM_005921.1:c.3094A>T	NP_005912.1:p.Asn1032Tyr
XM_005248519.3:c.2716A>T	XP_005248576.2:p.Asn906Tyr
XM_011543406.1:c.2839A>T	XP_011541708.1:p.Asn947Tyr
XM_011543407.1:c.2815A>T	XP_011541709.1:p.Asn939Tyr
XM_011543408.1:c.3094A>T	XP_011541710.1:p.Asn1032Tyr
XM_017009484.1:c.2683A>T	XP_016864973.1:p.Asn895Tyr
XM_017009485.1:c.2605A>T	XP_016864974.1:p.Asn869Tyr
XR_001742068.2:n.3125A>T
NM_005921.2:c.3094A>T MANE Select	NP_005912.1:p.Asn1032Tyr