Canonical Allele Identifier: CA359786353

Gene: MAP3K1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2675A>T MANE Select	ENSP00000382423.3:p.Asn892Ile
ENST00000399503.3:c.2675A>T	ENSP00000382423.3:p.Asn892Ile
NM_005921.1:c.2675A>T	NP_005912.1:p.Asn892Ile
XM_005248519.3:c.2297A>T	XP_005248576.2:p.Asn766Ile
XM_011543406.1:c.2420A>T	XP_011541708.1:p.Asn807Ile
XM_011543407.1:c.2396A>T	XP_011541709.1:p.Asn799Ile
XM_011543408.1:c.2675A>T	XP_011541710.1:p.Asn892Ile
XM_017009484.1:c.2264A>T	XP_016864973.1:p.Asn755Ile
XM_017009485.1:c.2186A>T	XP_016864974.1:p.Asn729Ile
XR_001742068.2:n.2706A>T
NM_005921.2:c.2675A>T MANE Select	NP_005912.1:p.Asn892Ile