Canonical Allele Identifier: CA444399861

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178162C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882335C>T , CM000667.2:g.56882335C>T	GRCh38
NC_000005.9:g.56178162C>T , CM000667.1:g.56178162C>T	GRCh37
NC_000005.8:g.56213919C>T	NCBI36
NG_031884.1:g.72263C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3135C>T MANE Select	ENSP00000382423.3:p.Val1045=
ENST00000399503.3:c.3135C>T	ENSP00000382423.3:p.Val1045=
NM_005921.1:c.3135C>T	NP_005912.1:p.Val1045=
XM_005248519.3:c.2757C>T	XP_005248576.2:p.Val919=
XM_011543406.1:c.2880C>T	XP_011541708.1:p.Val960=
XM_011543407.1:c.2856C>T	XP_011541709.1:p.Val952=
XM_011543408.1:c.3135C>T	XP_011541710.1:p.Val1045=
XM_017009484.1:c.2724C>T	XP_016864973.1:p.Val908=
XM_017009485.1:c.2646C>T	XP_016864974.1:p.Val882=
XR_001742068.2:n.3166C>T
NM_005921.2:c.3135C>T MANE Select	NP_005912.1:p.Val1045=