Canonical Allele Identifier: CA359787843

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178211C>A (hg19) ; chr5:g.56882384C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882384C>A , CM000667.2:g.56882384C>A	GRCh38
NC_000005.9:g.56178211C>A , CM000667.1:g.56178211C>A	GRCh37
NC_000005.8:g.56213968C>A	NCBI36
NG_031884.1:g.72312C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3184C>A MANE Select	ENSP00000382423.3:p.Pro1062Thr
ENST00000399503.3:c.3184C>A	ENSP00000382423.3:p.Pro1062Thr
NM_005921.1:c.3184C>A	NP_005912.1:p.Pro1062Thr
XM_005248519.3:c.2806C>A	XP_005248576.2:p.Pro936Thr
XM_011543406.1:c.2929C>A	XP_011541708.1:p.Pro977Thr
XM_011543407.1:c.2905C>A	XP_011541709.1:p.Pro969Thr
XM_011543408.1:c.3184C>A	XP_011541710.1:p.Pro1062Thr
XM_017009484.1:c.2773C>A	XP_016864973.1:p.Pro925Thr
XM_017009485.1:c.2695C>A	XP_016864974.1:p.Pro899Thr
XR_001742068.2:n.3215C>A
NM_005921.2:c.3184C>A MANE Select	NP_005912.1:p.Pro1062Thr