Canonical Allele Identifier: CA444399550

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178064A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882237A>C , CM000667.2:g.56882237A>C	GRCh38
NC_000005.9:g.56178064A>C , CM000667.1:g.56178064A>C	GRCh37
NC_000005.8:g.56213821A>C	NCBI36
NG_031884.1:g.72165A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3037A>C MANE Select	ENSP00000382423.3:p.Arg1013=
ENST00000399503.3:c.3037A>C	ENSP00000382423.3:p.Arg1013=
NM_005921.1:c.3037A>C	NP_005912.1:p.Arg1013=
XM_005248519.3:c.2659A>C	XP_005248576.2:p.Arg887=
XM_011543406.1:c.2782A>C	XP_011541708.1:p.Arg928=
XM_011543407.1:c.2758A>C	XP_011541709.1:p.Arg920=
XM_011543408.1:c.3037A>C	XP_011541710.1:p.Arg1013=
XM_017009484.1:c.2626A>C	XP_016864973.1:p.Arg876=
XM_017009485.1:c.2548A>C	XP_016864974.1:p.Arg850=
XR_001742068.2:n.3068A>C
NM_005921.2:c.3037A>C MANE Select	NP_005912.1:p.Arg1013=