Canonical Allele Identifier: CA359786339

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177700C>G (hg19) ; chr5:g.56881873C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881873C>G , CM000667.2:g.56881873C>G	GRCh38
NC_000005.9:g.56177700C>G , CM000667.1:g.56177700C>G	GRCh37
NC_000005.8:g.56213457C>G	NCBI36
NG_031884.1:g.71801C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2673C>G MANE Select	ENSP00000382423.3:p.Asn891Lys
ENST00000399503.3:c.2673C>G	ENSP00000382423.3:p.Asn891Lys
NM_005921.1:c.2673C>G	NP_005912.1:p.Asn891Lys
XM_005248519.3:c.2295C>G	XP_005248576.2:p.Asn765Lys
XM_011543406.1:c.2418C>G	XP_011541708.1:p.Asn806Lys
XM_011543407.1:c.2394C>G	XP_011541709.1:p.Asn798Lys
XM_011543408.1:c.2673C>G	XP_011541710.1:p.Asn891Lys
XM_017009484.1:c.2262C>G	XP_016864973.1:p.Asn754Lys
XM_017009485.1:c.2184C>G	XP_016864974.1:p.Asn728Lys
XR_001742068.2:n.2704C>G
NM_005921.2:c.2673C>G MANE Select	NP_005912.1:p.Asn891Lys