Canonical Allele Identifier: CA444399560

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945036
• MyVariant Identifiers: chr5:g.56178069A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882242A>T , CM000667.2:g.56882242A>T	GRCh38
NC_000005.9:g.56178069A>T , CM000667.1:g.56178069A>T	GRCh37
NC_000005.8:g.56213826A>T	NCBI36
NG_031884.1:g.72170A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3042A>T MANE Select	ENSP00000382423.3:p.Ile1014=
ENST00000399503.3:c.3042A>T	ENSP00000382423.3:p.Ile1014=
NM_005921.1:c.3042A>T	NP_005912.1:p.Ile1014=
XM_005248519.3:c.2664A>T	XP_005248576.2:p.Ile888=
XM_011543406.1:c.2787A>T	XP_011541708.1:p.Ile929=
XM_011543407.1:c.2763A>T	XP_011541709.1:p.Ile921=
XM_011543408.1:c.3042A>T	XP_011541710.1:p.Ile1014=
XM_017009484.1:c.2631A>T	XP_016864973.1:p.Ile877=
XM_017009485.1:c.2553A>T	XP_016864974.1:p.Ile851=
XR_001742068.2:n.3073A>T
NM_005921.2:c.3042A>T MANE Select	NP_005912.1:p.Ile1014=