Canonical Allele Identifier: CA359786202

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177654C>G (hg19) ; chr5:g.56881827C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881827C>G , CM000667.2:g.56881827C>G	GRCh38
NC_000005.9:g.56177654C>G , CM000667.1:g.56177654C>G	GRCh37
NC_000005.8:g.56213411C>G	NCBI36
NG_031884.1:g.71755C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2627C>G MANE Select	ENSP00000382423.3:p.Thr876Ser
ENST00000399503.3:c.2627C>G	ENSP00000382423.3:p.Thr876Ser
NM_005921.1:c.2627C>G	NP_005912.1:p.Thr876Ser
XM_005248519.3:c.2249C>G	XP_005248576.2:p.Thr750Ser
XM_011543406.1:c.2372C>G	XP_011541708.1:p.Thr791Ser
XM_011543407.1:c.2348C>G	XP_011541709.1:p.Thr783Ser
XM_011543408.1:c.2627C>G	XP_011541710.1:p.Thr876Ser
XM_017009484.1:c.2216C>G	XP_016864973.1:p.Thr739Ser
XM_017009485.1:c.2138C>G	XP_016864974.1:p.Thr713Ser
XR_001742068.2:n.2658C>G
NM_005921.2:c.2627C>G MANE Select	NP_005912.1:p.Thr876Ser