Canonical Allele Identifier: CA359786476

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177746C>G (hg19) ; chr5:g.56881919C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881919C>G , CM000667.2:g.56881919C>G	GRCh38
NC_000005.9:g.56177746C>G , CM000667.1:g.56177746C>G	GRCh37
NC_000005.8:g.56213503C>G	NCBI36
NG_031884.1:g.71847C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2719C>G MANE Select	ENSP00000382423.3:p.His907Asp
ENST00000399503.3:c.2719C>G	ENSP00000382423.3:p.His907Asp
NM_005921.1:c.2719C>G	NP_005912.1:p.His907Asp
XM_005248519.3:c.2341C>G	XP_005248576.2:p.His781Asp
XM_011543406.1:c.2464C>G	XP_011541708.1:p.His822Asp
XM_011543407.1:c.2440C>G	XP_011541709.1:p.His814Asp
XM_011543408.1:c.2719C>G	XP_011541710.1:p.His907Asp
XM_017009484.1:c.2308C>G	XP_016864973.1:p.His770Asp
XM_017009485.1:c.2230C>G	XP_016864974.1:p.His744Asp
XR_001742068.2:n.2750C>G
NM_005921.2:c.2719C>G MANE Select	NP_005912.1:p.His907Asp