Canonical Allele Identifier: CA359785894

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177509A>T (hg19) ; chr5:g.56881682A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881682A>T , CM000667.2:g.56881682A>T	GRCh38
NC_000005.9:g.56177509A>T , CM000667.1:g.56177509A>T	GRCh37
NC_000005.8:g.56213266A>T	NCBI36
NG_031884.1:g.71610A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2482A>T MANE Select	ENSP00000382423.3:p.Thr828Ser
ENST00000399503.3:c.2482A>T	ENSP00000382423.3:p.Thr828Ser
NM_005921.1:c.2482A>T	NP_005912.1:p.Thr828Ser
XM_005248519.3:c.2104A>T	XP_005248576.2:p.Thr702Ser
XM_011543406.1:c.2227A>T	XP_011541708.1:p.Thr743Ser
XM_011543407.1:c.2203A>T	XP_011541709.1:p.Thr735Ser
XM_011543408.1:c.2482A>T	XP_011541710.1:p.Thr828Ser
XM_017009484.1:c.2071A>T	XP_016864973.1:p.Thr691Ser
XM_017009485.1:c.1993A>T	XP_016864974.1:p.Thr665Ser
XR_001742068.2:n.2513A>T
NM_005921.2:c.2482A>T MANE Select	NP_005912.1:p.Thr828Ser