Canonical Allele Identifier: CA359787805

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111946209
• MyVariant Identifiers: chr5:g.56178194A>T (hg19) ; chr5:g.56882367A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882367A>T , CM000667.2:g.56882367A>T	GRCh38
NC_000005.9:g.56178194A>T , CM000667.1:g.56178194A>T	GRCh37
NC_000005.8:g.56213951A>T	NCBI36
NG_031884.1:g.72295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3167A>T MANE Select	ENSP00000382423.3:p.Asn1056Ile
ENST00000399503.3:c.3167A>T	ENSP00000382423.3:p.Asn1056Ile
NM_005921.1:c.3167A>T	NP_005912.1:p.Asn1056Ile
XM_005248519.3:c.2789A>T	XP_005248576.2:p.Asn930Ile
XM_011543406.1:c.2912A>T	XP_011541708.1:p.Asn971Ile
XM_011543407.1:c.2888A>T	XP_011541709.1:p.Asn963Ile
XM_011543408.1:c.3167A>T	XP_011541710.1:p.Asn1056Ile
XM_017009484.1:c.2756A>T	XP_016864973.1:p.Asn919Ile
XM_017009485.1:c.2678A>T	XP_016864974.1:p.Asn893Ile
XR_001742068.2:n.3198A>T
NM_005921.2:c.3167A>T MANE Select	NP_005912.1:p.Asn1056Ile