Canonical Allele Identifier: CA359802505

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56859808-C-G
• MyVariant Identifiers: chr5:g.56155635C>G (hg19) ; chr5:g.56859808C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859808C>G , CM000667.2:g.56859808C>G	GRCh38
NC_000005.9:g.56155635C>G , CM000667.1:g.56155635C>G	GRCh37
NC_000005.8:g.56191392C>G	NCBI36
NG_031884.1:g.49736C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.727C>G MANE Select	ENSP00000382423.3:p.Pro243Ala
ENST00000399503.3:c.727C>G	ENSP00000382423.3:p.Pro243Ala
NM_005921.1:c.727C>G	NP_005912.1:p.Pro243Ala
XM_005248519.3:c.349C>G	XP_005248576.2:p.Pro117Ala
XM_011543406.1:c.472C>G	XP_011541708.1:p.Pro158Ala
XM_011543407.1:c.727C>G	XP_011541709.1:p.Pro243Ala
XM_011543408.1:c.727C>G	XP_011541710.1:p.Pro243Ala
XM_017009484.1:c.316C>G	XP_016864973.1:p.Pro106Ala
XM_017009485.1:c.238C>G	XP_016864974.1:p.Pro80Ala
XR_001742068.2:n.758C>G
NM_005921.2:c.727C>G MANE Select	NP_005912.1:p.Pro243Ala