Canonical Allele Identifier: CA359787689

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945742
• MyVariant Identifiers: chr5:g.56178141C>G (hg19) ; chr5:g.56882314C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882314C>G , CM000667.2:g.56882314C>G	GRCh38
NC_000005.9:g.56178141C>G , CM000667.1:g.56178141C>G	GRCh37
NC_000005.8:g.56213898C>G	NCBI36
NG_031884.1:g.72242C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3114C>G MANE Select	ENSP00000382423.3:p.Asp1038Glu
ENST00000399503.3:c.3114C>G	ENSP00000382423.3:p.Asp1038Glu
NM_005921.1:c.3114C>G	NP_005912.1:p.Asp1038Glu
XM_005248519.3:c.2736C>G	XP_005248576.2:p.Asp912Glu
XM_011543406.1:c.2859C>G	XP_011541708.1:p.Asp953Glu
XM_011543407.1:c.2835C>G	XP_011541709.1:p.Asp945Glu
XM_011543408.1:c.3114C>G	XP_011541710.1:p.Asp1038Glu
XM_017009484.1:c.2703C>G	XP_016864973.1:p.Asp901Glu
XM_017009485.1:c.2625C>G	XP_016864974.1:p.Asp875Glu
XR_001742068.2:n.3145C>G
NM_005921.2:c.3114C>G MANE Select	NP_005912.1:p.Asp1038Glu