Canonical Allele Identifier: CA444399090

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177484C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881657C>T , CM000667.2:g.56881657C>T	GRCh38
NC_000005.9:g.56177484C>T , CM000667.1:g.56177484C>T	GRCh37
NC_000005.8:g.56213241C>T	NCBI36
NG_031884.1:g.71585C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2457C>T MANE Select	ENSP00000382423.3:p.Ile819=
ENST00000399503.3:c.2457C>T	ENSP00000382423.3:p.Ile819=
NM_005921.1:c.2457C>T	NP_005912.1:p.Ile819=
XM_005248519.3:c.2079C>T	XP_005248576.2:p.Ile693=
XM_011543406.1:c.2202C>T	XP_011541708.1:p.Ile734=
XM_011543407.1:c.2178C>T	XP_011541709.1:p.Ile726=
XM_011543408.1:c.2457C>T	XP_011541710.1:p.Ile819=
XM_017009484.1:c.2046C>T	XP_016864973.1:p.Ile682=
XM_017009485.1:c.1968C>T	XP_016864974.1:p.Ile656=
XR_001742068.2:n.2488C>T
NM_005921.2:c.2457C>T MANE Select	NP_005912.1:p.Ile819=