Canonical Allele Identifier: CA359802402

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155585A>C (hg19) ; chr5:g.56859758A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859758A>C , CM000667.2:g.56859758A>C	GRCh38
NC_000005.9:g.56155585A>C , CM000667.1:g.56155585A>C	GRCh37
NC_000005.8:g.56191342A>C	NCBI36
NG_031884.1:g.49686A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.677A>C MANE Select	ENSP00000382423.3:p.Asn226Thr
ENST00000399503.3:c.677A>C	ENSP00000382423.3:p.Asn226Thr
NM_005921.1:c.677A>C	NP_005912.1:p.Asn226Thr
XM_005248519.3:c.299A>C	XP_005248576.2:p.Asn100Thr
XM_011543406.1:c.422A>C	XP_011541708.1:p.Asn141Thr
XM_011543407.1:c.677A>C	XP_011541709.1:p.Asn226Thr
XM_011543408.1:c.677A>C	XP_011541710.1:p.Asn226Thr
XM_017009484.1:c.266A>C	XP_016864973.1:p.Asn89Thr
XM_017009485.1:c.188A>C	XP_016864974.1:p.Asn63Thr
XR_001742068.2:n.708A>C
NM_005921.2:c.677A>C MANE Select	NP_005912.1:p.Asn226Thr