Canonical Allele Identifier: CA359787741

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945992
• MyVariant Identifiers: chr5:g.56178166A>C (hg19) ; chr5:g.56882339A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882339A>C , CM000667.2:g.56882339A>C	GRCh38
NC_000005.9:g.56178166A>C , CM000667.1:g.56178166A>C	GRCh37
NC_000005.8:g.56213923A>C	NCBI36
NG_031884.1:g.72267A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3139A>C MANE Select	ENSP00000382423.3:p.Thr1047Pro
ENST00000399503.3:c.3139A>C	ENSP00000382423.3:p.Thr1047Pro
NM_005921.1:c.3139A>C	NP_005912.1:p.Thr1047Pro
XM_005248519.3:c.2761A>C	XP_005248576.2:p.Thr921Pro
XM_011543406.1:c.2884A>C	XP_011541708.1:p.Thr962Pro
XM_011543407.1:c.2860A>C	XP_011541709.1:p.Thr954Pro
XM_011543408.1:c.3139A>C	XP_011541710.1:p.Thr1047Pro
XM_017009484.1:c.2728A>C	XP_016864973.1:p.Thr910Pro
XM_017009485.1:c.2650A>C	XP_016864974.1:p.Thr884Pro
XR_001742068.2:n.3170A>C
NM_005921.2:c.3139A>C MANE Select	NP_005912.1:p.Thr1047Pro