Canonical Allele Identifier: CA359780692

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170937C>G (hg19) ; chr5:g.56875110C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875110C>G , CM000667.2:g.56875110C>G	GRCh38
NC_000005.9:g.56170937C>G , CM000667.1:g.56170937C>G	GRCh37
NC_000005.8:g.56206694C>G	NCBI36
NG_031884.1:g.65038C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1765C>G MANE Select	ENSP00000382423.3:p.His589Asp
ENST00000399503.3:c.1765C>G	ENSP00000382423.3:p.His589Asp
NM_005921.1:c.1765C>G	NP_005912.1:p.His589Asp
XM_005248519.3:c.1387C>G	XP_005248576.2:p.His463Asp
XM_011543406.1:c.1510C>G	XP_011541708.1:p.His504Asp
XM_011543407.1:c.1686+2105C>G	XP_011541709.1:n.1686+2105C>G
XM_011543408.1:c.1765C>G	XP_011541710.1:p.His589Asp
XM_017009484.1:c.1354C>G	XP_016864973.1:p.His452Asp
XM_017009485.1:c.1276C>G	XP_016864974.1:p.His426Asp
XR_001742068.2:n.1796C>G
NM_005921.2:c.1765C>G MANE Select	NP_005912.1:p.His589Asp