Canonical Allele Identifier: CA444391738

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155682A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859855A>G , CM000667.2:g.56859855A>G	GRCh38
NC_000005.9:g.56155682A>G , CM000667.1:g.56155682A>G	GRCh37
NC_000005.8:g.56191439A>G	NCBI36
NG_031884.1:g.49783A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.774A>G MANE Select	ENSP00000382423.3:p.Ser258=
ENST00000399503.3:c.774A>G	ENSP00000382423.3:p.Ser258=
NM_005921.1:c.774A>G	NP_005912.1:p.Ser258=
XM_005248519.3:c.396A>G	XP_005248576.2:p.Ser132=
XM_011543406.1:c.519A>G	XP_011541708.1:p.Ser173=
XM_011543407.1:c.774A>G	XP_011541709.1:p.Ser258=
XM_011543408.1:c.774A>G	XP_011541710.1:p.Ser258=
XM_017009484.1:c.363A>G	XP_016864973.1:p.Ser121=
XM_017009485.1:c.285A>G	XP_016864974.1:p.Ser95=
XR_001742068.2:n.805A>G
NM_005921.2:c.774A>G MANE Select	NP_005912.1:p.Ser258=