Canonical Allele Identifier: CA444398916

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170936C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875109C>A , CM000667.2:g.56875109C>A	GRCh38
NC_000005.9:g.56170936C>A , CM000667.1:g.56170936C>A	GRCh37
NC_000005.8:g.56206693C>A	NCBI36
NG_031884.1:g.65037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1764C>A MANE Select	ENSP00000382423.3:p.Ser588=
ENST00000399503.3:c.1764C>A	ENSP00000382423.3:p.Ser588=
NM_005921.1:c.1764C>A	NP_005912.1:p.Ser588=
XM_005248519.3:c.1386C>A	XP_005248576.2:p.Ser462=
XM_011543406.1:c.1509C>A	XP_011541708.1:p.Ser503=
XM_011543407.1:c.1686+2104C>A	XP_011541709.1:n.1686+2104C>A
XM_011543408.1:c.1764C>A	XP_011541710.1:p.Ser588=
XM_017009484.1:c.1353C>A	XP_016864973.1:p.Ser451=
XM_017009485.1:c.1275C>A	XP_016864974.1:p.Ser425=
XR_001742068.2:n.1795C>A
NM_005921.2:c.1764C>A MANE Select	NP_005912.1:p.Ser588=