Canonical Allele Identifier: CA359787885

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178233A>C (hg19) ; chr5:g.56882406A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882406A>C , CM000667.2:g.56882406A>C	GRCh38
NC_000005.9:g.56178233A>C , CM000667.1:g.56178233A>C	GRCh37
NC_000005.8:g.56213990A>C	NCBI36
NG_031884.1:g.72334A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3206A>C MANE Select	ENSP00000382423.3:p.Asn1069Thr
ENST00000399503.3:c.3206A>C	ENSP00000382423.3:p.Asn1069Thr
NM_005921.1:c.3206A>C	NP_005912.1:p.Asn1069Thr
XM_005248519.3:c.2828A>C	XP_005248576.2:p.Asn943Thr
XM_011543406.1:c.2951A>C	XP_011541708.1:p.Asn984Thr
XM_011543407.1:c.2927A>C	XP_011541709.1:p.Asn976Thr
XM_011543408.1:c.3206A>C	XP_011541710.1:p.Asn1069Thr
XM_017009484.1:c.2795A>C	XP_016864973.1:p.Asn932Thr
XM_017009485.1:c.2717A>C	XP_016864974.1:p.Asn906Thr
XR_001742068.2:n.3237A>C
NM_005921.2:c.3206A>C MANE Select	NP_005912.1:p.Asn1069Thr