Canonical Allele Identifier: CA359787683

Gene: MAP3K1

Linked Data

• dbSNP Id: rs377648645
• MyVariant Identifiers: chr5:g.56178139G>A (hg19) ; chr5:g.56882312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882312G>A , CM000667.2:g.56882312G>A	GRCh38
NC_000005.9:g.56178139G>A , CM000667.1:g.56178139G>A	GRCh37
NC_000005.8:g.56213896G>A	NCBI36
NG_031884.1:g.72240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3112G>A MANE Select	ENSP00000382423.3:p.Asp1038Asn
ENST00000399503.3:c.3112G>A	ENSP00000382423.3:p.Asp1038Asn
NM_005921.1:c.3112G>A	NP_005912.1:p.Asp1038Asn
XM_005248519.3:c.2734G>A	XP_005248576.2:p.Asp912Asn
XM_011543406.1:c.2857G>A	XP_011541708.1:p.Asp953Asn
XM_011543407.1:c.2833G>A	XP_011541709.1:p.Asp945Asn
XM_011543408.1:c.3112G>A	XP_011541710.1:p.Asp1038Asn
XM_017009484.1:c.2701G>A	XP_016864973.1:p.Asp901Asn
XM_017009485.1:c.2623G>A	XP_016864974.1:p.Asp875Asn
XR_001742068.2:n.3143G>A
NM_005921.2:c.3112G>A MANE Select	NP_005912.1:p.Asp1038Asn