Canonical Allele Identifier: CA444399553

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1488304768
• gnomAD v3: 5-56882410-A-C
• gnomAD v4: 5-56882410-A-C
• MyVariant Identifiers: chr5:g.56178237A>C (hg19) ; chr5:g.56882410A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882410A>C , CM000667.2:g.56882410A>C	GRCh38
NC_000005.9:g.56178237A>C , CM000667.1:g.56178237A>C	GRCh37
NC_000005.8:g.56213994A>C	NCBI36
NG_031884.1:g.72338A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3210A>C MANE Select	ENSP00000382423.3:p.Thr1070=
ENST00000399503.3:c.3210A>C	ENSP00000382423.3:p.Thr1070=
NM_005921.1:c.3210A>C	NP_005912.1:p.Thr1070=
XM_005248519.3:c.2832A>C	XP_005248576.2:p.Thr944=
XM_011543406.1:c.2955A>C	XP_011541708.1:p.Thr985=
XM_011543407.1:c.2931A>C	XP_011541709.1:p.Thr977=
XM_011543408.1:c.3210A>C	XP_011541710.1:p.Thr1070=
XM_017009484.1:c.2799A>C	XP_016864973.1:p.Thr933=
XM_017009485.1:c.2721A>C	XP_016864974.1:p.Thr907=
XR_001742068.2:n.3241A>C
NM_005921.2:c.3210A>C MANE Select	NP_005912.1:p.Thr1070=