Canonical Allele Identifier: CA359786775

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1748229636
• gnomAD v4: 5-56882042-A-G
• MyVariant Identifiers: chr5:g.56177869A>G (hg19) ; chr5:g.56882042A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882042A>G , CM000667.2:g.56882042A>G	GRCh38
NC_000005.9:g.56177869A>G , CM000667.1:g.56177869A>G	GRCh37
NC_000005.8:g.56213626A>G	NCBI36
NG_031884.1:g.71970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2842A>G MANE Select	ENSP00000382423.3:p.Thr948Ala
ENST00000399503.3:c.2842A>G	ENSP00000382423.3:p.Thr948Ala
NM_005921.1:c.2842A>G	NP_005912.1:p.Thr948Ala
XM_005248519.3:c.2464A>G	XP_005248576.2:p.Thr822Ala
XM_011543406.1:c.2587A>G	XP_011541708.1:p.Thr863Ala
XM_011543407.1:c.2563A>G	XP_011541709.1:p.Thr855Ala
XM_011543408.1:c.2842A>G	XP_011541710.1:p.Thr948Ala
XM_017009484.1:c.2431A>G	XP_016864973.1:p.Thr811Ala
XM_017009485.1:c.2353A>G	XP_016864974.1:p.Thr785Ala
XR_001742068.2:n.2873A>G
NM_005921.2:c.2842A>G MANE Select	NP_005912.1:p.Thr948Ala