Canonical Allele Identifier: CA359787004

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177920C>T (hg19) ; chr5:g.56882093C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882093C>T , CM000667.2:g.56882093C>T	GRCh38
NC_000005.9:g.56177920C>T , CM000667.1:g.56177920C>T	GRCh37
NC_000005.8:g.56213677C>T	NCBI36
NG_031884.1:g.72021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2893C>T MANE Select	ENSP00000382423.3:p.Gln965Ter
ENST00000399503.3:c.2893C>T	ENSP00000382423.3:p.Gln965Ter
NM_005921.1:c.2893C>T	NP_005912.1:p.Gln965Ter
XM_005248519.3:c.2515C>T	XP_005248576.2:p.Gln839Ter
XM_011543406.1:c.2638C>T	XP_011541708.1:p.Gln880Ter
XM_011543407.1:c.2614C>T	XP_011541709.1:p.Gln872Ter
XM_011543408.1:c.2893C>T	XP_011541710.1:p.Gln965Ter
XM_017009484.1:c.2482C>T	XP_016864973.1:p.Gln828Ter
XM_017009485.1:c.2404C>T	XP_016864974.1:p.Gln802Ter
XR_001742068.2:n.2924C>T
NM_005921.2:c.2893C>T MANE Select	NP_005912.1:p.Gln965Ter