Canonical Allele Identifier: CA359780997

Gene: MAP3K1

Linked Data

• dbSNP Id: rs758597381
• MyVariant Identifiers: chr5:g.56171017T>G (hg19) ; chr5:g.56875190T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875190T>G , CM000667.2:g.56875190T>G	GRCh38
NC_000005.9:g.56171017T>G , CM000667.1:g.56171017T>G	GRCh37
NC_000005.8:g.56206774T>G	NCBI36
NG_031884.1:g.65118T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1845T>G MANE Select	ENSP00000382423.3:p.Ser615Arg
ENST00000399503.3:c.1845T>G	ENSP00000382423.3:p.Ser615Arg
NM_005921.1:c.1845T>G	NP_005912.1:p.Ser615Arg
XM_005248519.3:c.1467T>G	XP_005248576.2:p.Ser489Arg
XM_011543406.1:c.1590T>G	XP_011541708.1:p.Ser530Arg
XM_011543407.1:c.1686+2185T>G	XP_011541709.1:n.1686+2185T>G
XM_011543408.1:c.1845T>G	XP_011541710.1:p.Ser615Arg
XM_017009484.1:c.1434T>G	XP_016864973.1:p.Ser478Arg
XM_017009485.1:c.1356T>G	XP_016864974.1:p.Ser452Arg
XR_001742068.2:n.1876T>G
NM_005921.2:c.1845T>G MANE Select	NP_005912.1:p.Ser615Arg