Canonical Allele Identifier: CA359787804

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111946209
• MyVariant Identifiers: chr5:g.56178194A>C (hg19) ; chr5:g.56882367A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882367A>C , CM000667.2:g.56882367A>C	GRCh38
NC_000005.9:g.56178194A>C , CM000667.1:g.56178194A>C	GRCh37
NC_000005.8:g.56213951A>C	NCBI36
NG_031884.1:g.72295A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3167A>C MANE Select	ENSP00000382423.3:p.Asn1056Thr
ENST00000399503.3:c.3167A>C	ENSP00000382423.3:p.Asn1056Thr
NM_005921.1:c.3167A>C	NP_005912.1:p.Asn1056Thr
XM_005248519.3:c.2789A>C	XP_005248576.2:p.Asn930Thr
XM_011543406.1:c.2912A>C	XP_011541708.1:p.Asn971Thr
XM_011543407.1:c.2888A>C	XP_011541709.1:p.Asn963Thr
XM_011543408.1:c.3167A>C	XP_011541710.1:p.Asn1056Thr
XM_017009484.1:c.2756A>C	XP_016864973.1:p.Asn919Thr
XM_017009485.1:c.2678A>C	XP_016864974.1:p.Asn893Thr
XR_001742068.2:n.3198A>C
NM_005921.2:c.3167A>C MANE Select	NP_005912.1:p.Asn1056Thr