Canonical Allele Identifier: CA444391765

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155715A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859888A>C , CM000667.2:g.56859888A>C	GRCh38
NC_000005.9:g.56155715A>C , CM000667.1:g.56155715A>C	GRCh37
NC_000005.8:g.56191472A>C	NCBI36
NG_031884.1:g.49816A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.807A>C MANE Select	ENSP00000382423.3:p.Val269=
ENST00000399503.3:c.807A>C	ENSP00000382423.3:p.Val269=
NM_005921.1:c.807A>C	NP_005912.1:p.Val269=
XM_005248519.3:c.429A>C	XP_005248576.2:p.Val143=
XM_011543406.1:c.552A>C	XP_011541708.1:p.Val184=
XM_011543407.1:c.807A>C	XP_011541709.1:p.Val269=
XM_011543408.1:c.807A>C	XP_011541710.1:p.Val269=
XM_017009484.1:c.396A>C	XP_016864973.1:p.Val132=
XM_017009485.1:c.318A>C	XP_016864974.1:p.Val106=
XR_001742068.2:n.838A>C
NM_005921.2:c.807A>C MANE Select	NP_005912.1:p.Val269=