Canonical Allele Identifier: CA359786466

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177740A>G (hg19) ; chr5:g.56881913A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881913A>G , CM000667.2:g.56881913A>G	GRCh38
NC_000005.9:g.56177740A>G , CM000667.1:g.56177740A>G	GRCh37
NC_000005.8:g.56213497A>G	NCBI36
NG_031884.1:g.71841A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2713A>G MANE Select	ENSP00000382423.3:p.Thr905Ala
ENST00000399503.3:c.2713A>G	ENSP00000382423.3:p.Thr905Ala
NM_005921.1:c.2713A>G	NP_005912.1:p.Thr905Ala
XM_005248519.3:c.2335A>G	XP_005248576.2:p.Thr779Ala
XM_011543406.1:c.2458A>G	XP_011541708.1:p.Thr820Ala
XM_011543407.1:c.2434A>G	XP_011541709.1:p.Thr812Ala
XM_011543408.1:c.2713A>G	XP_011541710.1:p.Thr905Ala
XM_017009484.1:c.2302A>G	XP_016864973.1:p.Thr768Ala
XM_017009485.1:c.2224A>G	XP_016864974.1:p.Thr742Ala
XR_001742068.2:n.2744A>G
NM_005921.2:c.2713A>G MANE Select	NP_005912.1:p.Thr905Ala