Canonical Allele Identifier: CA444399134

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177550G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881723G>C , CM000667.2:g.56881723G>C	GRCh38
NC_000005.9:g.56177550G>C , CM000667.1:g.56177550G>C	GRCh37
NC_000005.8:g.56213307G>C	NCBI36
NG_031884.1:g.71651G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2523G>C MANE Select	ENSP00000382423.3:p.Leu841=
ENST00000399503.3:c.2523G>C	ENSP00000382423.3:p.Leu841=
NM_005921.1:c.2523G>C	NP_005912.1:p.Leu841=
XM_005248519.3:c.2145G>C	XP_005248576.2:p.Leu715=
XM_011543406.1:c.2268G>C	XP_011541708.1:p.Leu756=
XM_011543407.1:c.2244G>C	XP_011541709.1:p.Leu748=
XM_011543408.1:c.2523G>C	XP_011541710.1:p.Leu841=
XM_017009484.1:c.2112G>C	XP_016864973.1:p.Leu704=
XM_017009485.1:c.2034G>C	XP_016864974.1:p.Leu678=
XR_001742068.2:n.2554G>C
NM_005921.2:c.2523G>C MANE Select	NP_005912.1:p.Leu841=