Canonical Allele Identifier: CA444398915

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171116C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875289C>T , CM000667.2:g.56875289C>T	GRCh38
NC_000005.9:g.56171116C>T , CM000667.1:g.56171116C>T	GRCh37
NC_000005.8:g.56206873C>T	NCBI36
NG_031884.1:g.65217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1944C>T MANE Select	ENSP00000382423.3:p.Tyr648=
ENST00000399503.3:c.1944C>T	ENSP00000382423.3:p.Tyr648=
NM_005921.1:c.1944C>T	NP_005912.1:p.Tyr648=
XM_005248519.3:c.1566C>T	XP_005248576.2:p.Tyr522=
XM_011543406.1:c.1689C>T	XP_011541708.1:p.Tyr563=
XM_011543407.1:c.1686+2284C>T	XP_011541709.1:n.1686+2284C>T
XM_011543408.1:c.1944C>T	XP_011541710.1:p.Tyr648=
XM_017009484.1:c.1533C>T	XP_016864973.1:p.Tyr511=
XM_017009485.1:c.1455C>T	XP_016864974.1:p.Tyr485=
XR_001742068.2:n.1975C>T
NM_005921.2:c.1944C>T MANE Select	NP_005912.1:p.Tyr648=