Canonical Allele Identifier: CA359780912

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111921002
• MyVariant Identifiers: chr5:g.56171001G>A (hg19) ; chr5:g.56875174G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875174G>A , CM000667.2:g.56875174G>A	GRCh38
NC_000005.9:g.56171001G>A , CM000667.1:g.56171001G>A	GRCh37
NC_000005.8:g.56206758G>A	NCBI36
NG_031884.1:g.65102G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1829G>A MANE Select	ENSP00000382423.3:p.Ser610Asn
ENST00000399503.3:c.1829G>A	ENSP00000382423.3:p.Ser610Asn
NM_005921.1:c.1829G>A	NP_005912.1:p.Ser610Asn
XM_005248519.3:c.1451G>A	XP_005248576.2:p.Ser484Asn
XM_011543406.1:c.1574G>A	XP_011541708.1:p.Ser525Asn
XM_011543407.1:c.1686+2169G>A	XP_011541709.1:n.1686+2169G>A
XM_011543408.1:c.1829G>A	XP_011541710.1:p.Ser610Asn
XM_017009484.1:c.1418G>A	XP_016864973.1:p.Ser473Asn
XM_017009485.1:c.1340G>A	XP_016864974.1:p.Ser447Asn
XR_001742068.2:n.1860G>A
NM_005921.2:c.1829G>A MANE Select	NP_005912.1:p.Ser610Asn