Canonical Allele Identifier: CA444391785

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155739G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859912G>T , CM000667.2:g.56859912G>T	GRCh38
NC_000005.9:g.56155739G>T , CM000667.1:g.56155739G>T	GRCh37
NC_000005.8:g.56191496G>T	NCBI36
NG_031884.1:g.49840G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.831G>T MANE Select	ENSP00000382423.3:p.Val277=
ENST00000399503.3:c.831G>T	ENSP00000382423.3:p.Val277=
NM_005921.1:c.831G>T	NP_005912.1:p.Val277=
XM_005248519.3:c.453G>T	XP_005248576.2:p.Val151=
XM_011543406.1:c.576G>T	XP_011541708.1:p.Val192=
XM_011543407.1:c.831G>T	XP_011541709.1:p.Val277=
XM_011543408.1:c.831G>T	XP_011541710.1:p.Val277=
XM_017009484.1:c.420G>T	XP_016864973.1:p.Val140=
XM_017009485.1:c.342G>T	XP_016864974.1:p.Val114=
XR_001742068.2:n.862G>T
NM_005921.2:c.831G>T MANE Select	NP_005912.1:p.Val277=