Canonical Allele Identifier: CA359786448

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177732C>G (hg19) ; chr5:g.56881905C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881905C>G , CM000667.2:g.56881905C>G	GRCh38
NC_000005.9:g.56177732C>G , CM000667.1:g.56177732C>G	GRCh37
NC_000005.8:g.56213489C>G	NCBI36
NG_031884.1:g.71833C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2705C>G MANE Select	ENSP00000382423.3:p.Pro902Arg
ENST00000399503.3:c.2705C>G	ENSP00000382423.3:p.Pro902Arg
NM_005921.1:c.2705C>G	NP_005912.1:p.Pro902Arg
XM_005248519.3:c.2327C>G	XP_005248576.2:p.Pro776Arg
XM_011543406.1:c.2450C>G	XP_011541708.1:p.Pro817Arg
XM_011543407.1:c.2426C>G	XP_011541709.1:p.Pro809Arg
XM_011543408.1:c.2705C>G	XP_011541710.1:p.Pro902Arg
XM_017009484.1:c.2294C>G	XP_016864973.1:p.Pro765Arg
XM_017009485.1:c.2216C>G	XP_016864974.1:p.Pro739Arg
XR_001742068.2:n.2736C>G
NM_005921.2:c.2705C>G MANE Select	NP_005912.1:p.Pro902Arg