Canonical Allele Identifier: CA359787866

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56882396-A-G
• COSMIC: COSM3855706
• MyVariant Identifiers: chr5:g.56178223A>G (hg19) ; chr5:g.56882396A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882396A>G , CM000667.2:g.56882396A>G	GRCh38
NC_000005.9:g.56178223A>G , CM000667.1:g.56178223A>G	GRCh37
NC_000005.8:g.56213980A>G	NCBI36
NG_031884.1:g.72324A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3196A>G MANE Select	ENSP00000382423.3:p.Thr1066Ala
ENST00000399503.3:c.3196A>G	ENSP00000382423.3:p.Thr1066Ala
NM_005921.1:c.3196A>G	NP_005912.1:p.Thr1066Ala
XM_005248519.3:c.2818A>G	XP_005248576.2:p.Thr940Ala
XM_011543406.1:c.2941A>G	XP_011541708.1:p.Thr981Ala
XM_011543407.1:c.2917A>G	XP_011541709.1:p.Thr973Ala
XM_011543408.1:c.3196A>G	XP_011541710.1:p.Thr1066Ala
XM_017009484.1:c.2785A>G	XP_016864973.1:p.Thr929Ala
XM_017009485.1:c.2707A>G	XP_016864974.1:p.Thr903Ala
XR_001742068.2:n.3227A>G
NM_005921.2:c.3196A>G MANE Select	NP_005912.1:p.Thr1066Ala