Canonical Allele Identifier: CA359786115

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177613G>T (hg19) ; chr5:g.56881786G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881786G>T , CM000667.2:g.56881786G>T	GRCh38
NC_000005.9:g.56177613G>T , CM000667.1:g.56177613G>T	GRCh37
NC_000005.8:g.56213370G>T	NCBI36
NG_031884.1:g.71714G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2586G>T MANE Select	ENSP00000382423.3:p.Glu862Asp
ENST00000399503.3:c.2586G>T	ENSP00000382423.3:p.Glu862Asp
NM_005921.1:c.2586G>T	NP_005912.1:p.Glu862Asp
XM_005248519.3:c.2208G>T	XP_005248576.2:p.Glu736Asp
XM_011543406.1:c.2331G>T	XP_011541708.1:p.Glu777Asp
XM_011543407.1:c.2307G>T	XP_011541709.1:p.Glu769Asp
XM_011543408.1:c.2586G>T	XP_011541710.1:p.Glu862Asp
XM_017009484.1:c.2175G>T	XP_016864973.1:p.Glu725Asp
XM_017009485.1:c.2097G>T	XP_016864974.1:p.Glu699Asp
XR_001742068.2:n.2617G>T
NM_005921.2:c.2586G>T MANE Select	NP_005912.1:p.Glu862Asp