Canonical Allele Identifier: CA359786229

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177667A>T (hg19) ; chr5:g.56881840A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881840A>T , CM000667.2:g.56881840A>T	GRCh38
NC_000005.9:g.56177667A>T , CM000667.1:g.56177667A>T	GRCh37
NC_000005.8:g.56213424A>T	NCBI36
NG_031884.1:g.71768A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2640A>T MANE Select	ENSP00000382423.3:p.Gln880His
ENST00000399503.3:c.2640A>T	ENSP00000382423.3:p.Gln880His
NM_005921.1:c.2640A>T	NP_005912.1:p.Gln880His
XM_005248519.3:c.2262A>T	XP_005248576.2:p.Gln754His
XM_011543406.1:c.2385A>T	XP_011541708.1:p.Gln795His
XM_011543407.1:c.2361A>T	XP_011541709.1:p.Gln787His
XM_011543408.1:c.2640A>T	XP_011541710.1:p.Gln880His
XM_017009484.1:c.2229A>T	XP_016864973.1:p.Gln743His
XM_017009485.1:c.2151A>T	XP_016864974.1:p.Gln717His
XR_001742068.2:n.2671A>T
NM_005921.2:c.2640A>T MANE Select	NP_005912.1:p.Gln880His