Canonical Allele Identifier: CA359786623

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111942959
• MyVariant Identifiers: chr5:g.56177810C>A (hg19) ; chr5:g.56881983C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881983C>A , CM000667.2:g.56881983C>A	GRCh38
NC_000005.9:g.56177810C>A , CM000667.1:g.56177810C>A	GRCh37
NC_000005.8:g.56213567C>A	NCBI36
NG_031884.1:g.71911C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2783C>A MANE Select	ENSP00000382423.3:p.Ser928Tyr
ENST00000399503.3:c.2783C>A	ENSP00000382423.3:p.Ser928Tyr
NM_005921.1:c.2783C>A	NP_005912.1:p.Ser928Tyr
XM_005248519.3:c.2405C>A	XP_005248576.2:p.Ser802Tyr
XM_011543406.1:c.2528C>A	XP_011541708.1:p.Ser843Tyr
XM_011543407.1:c.2504C>A	XP_011541709.1:p.Ser835Tyr
XM_011543408.1:c.2783C>A	XP_011541710.1:p.Ser928Tyr
XM_017009484.1:c.2372C>A	XP_016864973.1:p.Ser791Tyr
XM_017009485.1:c.2294C>A	XP_016864974.1:p.Ser765Tyr
XR_001742068.2:n.2814C>A
NM_005921.2:c.2783C>A MANE Select	NP_005912.1:p.Ser928Tyr