Canonical Allele Identifier: CA444399201

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177703C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881876C>T , CM000667.2:g.56881876C>T	GRCh38
NC_000005.9:g.56177703C>T , CM000667.1:g.56177703C>T	GRCh37
NC_000005.8:g.56213460C>T	NCBI36
NG_031884.1:g.71804C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2676C>T MANE Select	ENSP00000382423.3:p.Asn892=
ENST00000399503.3:c.2676C>T	ENSP00000382423.3:p.Asn892=
NM_005921.1:c.2676C>T	NP_005912.1:p.Asn892=
XM_005248519.3:c.2298C>T	XP_005248576.2:p.Asn766=
XM_011543406.1:c.2421C>T	XP_011541708.1:p.Asn807=
XM_011543407.1:c.2397C>T	XP_011541709.1:p.Asn799=
XM_011543408.1:c.2676C>T	XP_011541710.1:p.Asn892=
XM_017009484.1:c.2265C>T	XP_016864973.1:p.Asn755=
XM_017009485.1:c.2187C>T	XP_016864974.1:p.Asn729=
XR_001742068.2:n.2707C>T
NM_005921.2:c.2676C>T MANE Select	NP_005912.1:p.Asn892=