Canonical Allele Identifier: CA444398992

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111920970
• MyVariant Identifiers: chr5:g.56170996C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875169C>G , CM000667.2:g.56875169C>G	GRCh38
NC_000005.9:g.56170996C>G , CM000667.1:g.56170996C>G	GRCh37
NC_000005.8:g.56206753C>G	NCBI36
NG_031884.1:g.65097C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1824C>G MANE Select	ENSP00000382423.3:p.Gly608=
ENST00000399503.3:c.1824C>G	ENSP00000382423.3:p.Gly608=
NM_005921.1:c.1824C>G	NP_005912.1:p.Gly608=
XM_005248519.3:c.1446C>G	XP_005248576.2:p.Gly482=
XM_011543406.1:c.1569C>G	XP_011541708.1:p.Gly523=
XM_011543407.1:c.1686+2164C>G	XP_011541709.1:n.1686+2164C>G
XM_011543408.1:c.1824C>G	XP_011541710.1:p.Gly608=
XM_017009484.1:c.1413C>G	XP_016864973.1:p.Gly471=
XM_017009485.1:c.1335C>G	XP_016864974.1:p.Gly445=
XR_001742068.2:n.1855C>G
NM_005921.2:c.1824C>G MANE Select	NP_005912.1:p.Gly608=