Canonical Allele Identifier: CA359787803

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178194A>G (hg19) ; chr5:g.56882367A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3167A>G MANE Select	ENSP00000382423.3:p.Asn1056Ser
ENST00000399503.3:c.3167A>G	ENSP00000382423.3:p.Asn1056Ser
NM_005921.1:c.3167A>G	NP_005912.1:p.Asn1056Ser
XM_005248519.3:c.2789A>G	XP_005248576.2:p.Asn930Ser
XM_011543406.1:c.2912A>G	XP_011541708.1:p.Asn971Ser
XM_011543407.1:c.2888A>G	XP_011541709.1:p.Asn963Ser
XM_011543408.1:c.3167A>G	XP_011541710.1:p.Asn1056Ser
XM_017009484.1:c.2756A>G	XP_016864973.1:p.Asn919Ser
XM_017009485.1:c.2678A>G	XP_016864974.1:p.Asn893Ser
XR_001742068.2:n.3198A>G
NM_005921.2:c.3167A>G MANE Select	NP_005912.1:p.Asn1056Ser