Canonical Allele Identifier: CA359786222

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177665C>T (hg19) ; chr5:g.56881838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881838C>T , CM000667.2:g.56881838C>T	GRCh38
NC_000005.9:g.56177665C>T , CM000667.1:g.56177665C>T	GRCh37
NC_000005.8:g.56213422C>T	NCBI36
NG_031884.1:g.71766C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2638C>T MANE Select	ENSP00000382423.3:p.Gln880Ter
ENST00000399503.3:c.2638C>T	ENSP00000382423.3:p.Gln880Ter
NM_005921.1:c.2638C>T	NP_005912.1:p.Gln880Ter
XM_005248519.3:c.2260C>T	XP_005248576.2:p.Gln754Ter
XM_011543406.1:c.2383C>T	XP_011541708.1:p.Gln795Ter
XM_011543407.1:c.2359C>T	XP_011541709.1:p.Gln787Ter
XM_011543408.1:c.2638C>T	XP_011541710.1:p.Gln880Ter
XM_017009484.1:c.2227C>T	XP_016864973.1:p.Gln743Ter
XM_017009485.1:c.2149C>T	XP_016864974.1:p.Gln717Ter
XR_001742068.2:n.2669C>T
NM_005921.2:c.2638C>T MANE Select	NP_005912.1:p.Gln880Ter