Canonical Allele Identifier: CA812351464

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1308928391
• MyVariant Identifiers: chr5:g.56177269A>C (hg19) ; chr5:g.56881442A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881442A>C , CM000667.2:g.56881442A>C	GRCh38
NC_000005.9:g.56177269A>C , CM000667.1:g.56177269A>C	GRCh37
NC_000005.8:g.56213026A>C	NCBI36
NG_031884.1:g.71370A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2370-128A>C MANE Select	ENSP00000382423.3:n.2370-128A>C
ENST00000399503.3:c.2370-128A>C	ENSP00000382423.3:n.2370-128A>C
NM_005921.1:c.2370-128A>C	NP_005912.1:n.2370-128A>C
XM_005248519.3:c.1992-128A>C	XP_005248576.2:n.1992-128A>C
XM_011543406.1:c.2115-128A>C	XP_011541708.1:n.2115-128A>C
XM_011543407.1:c.2091-128A>C	XP_011541709.1:n.2091-128A>C
XM_011543408.1:c.2370-128A>C	XP_011541710.1:n.2370-128A>C
XM_017009484.1:c.1959-128A>C	XP_016864973.1:n.1959-128A>C
XM_017009485.1:c.1881-128A>C	XP_016864974.1:n.1881-128A>C
XR_001742068.2:n.2401-128A>C
NM_005921.2:c.2370-128A>C MANE Select	NP_005912.1:n.2370-128A>C