Canonical Allele Identifier: CA359787623

Gene: MAP3K1

Linked Data

• dbSNP Id: rs146112116
• MyVariant Identifiers: chr5:g.56178114C>A (hg19) ; chr5:g.56882287C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882287C>A , CM000667.2:g.56882287C>A	GRCh38
NC_000005.9:g.56178114C>A , CM000667.1:g.56178114C>A	GRCh37
NC_000005.8:g.56213871C>A	NCBI36
NG_031884.1:g.72215C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3087C>A MANE Select	ENSP00000382423.3:p.Phe1029Leu
ENST00000399503.3:c.3087C>A	ENSP00000382423.3:p.Phe1029Leu
NM_005921.1:c.3087C>A	NP_005912.1:p.Phe1029Leu
XM_005248519.3:c.2709C>A	XP_005248576.2:p.Phe903Leu
XM_011543406.1:c.2832C>A	XP_011541708.1:p.Phe944Leu
XM_011543407.1:c.2808C>A	XP_011541709.1:p.Phe936Leu
XM_011543408.1:c.3087C>A	XP_011541710.1:p.Phe1029Leu
XM_017009484.1:c.2676C>A	XP_016864973.1:p.Phe892Leu
XM_017009485.1:c.2598C>A	XP_016864974.1:p.Phe866Leu
XR_001742068.2:n.3118C>A
NM_005921.2:c.3087C>A MANE Select	NP_005912.1:p.Phe1029Leu