Canonical Allele Identifier: CA359786351

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177702A>G (hg19) ; chr5:g.56881875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881875A>G , CM000667.2:g.56881875A>G	GRCh38
NC_000005.9:g.56177702A>G , CM000667.1:g.56177702A>G	GRCh37
NC_000005.8:g.56213459A>G	NCBI36
NG_031884.1:g.71803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2675A>G MANE Select	ENSP00000382423.3:p.Asn892Ser
ENST00000399503.3:c.2675A>G	ENSP00000382423.3:p.Asn892Ser
NM_005921.1:c.2675A>G	NP_005912.1:p.Asn892Ser
XM_005248519.3:c.2297A>G	XP_005248576.2:p.Asn766Ser
XM_011543406.1:c.2420A>G	XP_011541708.1:p.Asn807Ser
XM_011543407.1:c.2396A>G	XP_011541709.1:p.Asn799Ser
XM_011543408.1:c.2675A>G	XP_011541710.1:p.Asn892Ser
XM_017009484.1:c.2264A>G	XP_016864973.1:p.Asn755Ser
XM_017009485.1:c.2186A>G	XP_016864974.1:p.Asn729Ser
XR_001742068.2:n.2706A>G
NM_005921.2:c.2675A>G MANE Select	NP_005912.1:p.Asn892Ser