Canonical Allele Identifier: CA359802609

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155689A>G (hg19) ; chr5:g.56859862A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859862A>G , CM000667.2:g.56859862A>G	GRCh38
NC_000005.9:g.56155689A>G , CM000667.1:g.56155689A>G	GRCh37
NC_000005.8:g.56191446A>G	NCBI36
NG_031884.1:g.49790A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.781A>G MANE Select	ENSP00000382423.3:p.Thr261Ala
ENST00000399503.3:c.781A>G	ENSP00000382423.3:p.Thr261Ala
NM_005921.1:c.781A>G	NP_005912.1:p.Thr261Ala
XM_005248519.3:c.403A>G	XP_005248576.2:p.Thr135Ala
XM_011543406.1:c.526A>G	XP_011541708.1:p.Thr176Ala
XM_011543407.1:c.781A>G	XP_011541709.1:p.Thr261Ala
XM_011543408.1:c.781A>G	XP_011541710.1:p.Thr261Ala
XM_017009484.1:c.370A>G	XP_016864973.1:p.Thr124Ala
XM_017009485.1:c.292A>G	XP_016864974.1:p.Thr98Ala
XR_001742068.2:n.812A>G
NM_005921.2:c.781A>G MANE Select	NP_005912.1:p.Thr261Ala