Canonical Allele Identifier: CA444398995
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111920985
MyVariant Identifiers: chr5:g.56170999C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875172C>T , CM000667.2:g.56875172C>T GRCh38
NC_000005.9:g.56170999C>T , CM000667.1:g.56170999C>T GRCh37
NC_000005.8:g.56206756C>T NCBI36
NG_031884.1:g.65100C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1827C>T MANE Select ENSP00000382423.3:p.Ser609=
ENST00000399503.3:c.1827C>T ENSP00000382423.3:p.Ser609=
NM_005921.1:c.1827C>T NP_005912.1:p.Ser609=
XM_005248519.3:c.1449C>T XP_005248576.2:p.Ser483=
XM_011543406.1:c.1572C>T XP_011541708.1:p.Ser524=
XM_011543407.1:c.1686+2167C>T XP_011541709.1:n.1686+2167C>T
XM_011543408.1:c.1827C>T XP_011541710.1:p.Ser609=
XM_017009484.1:c.1416C>T XP_016864973.1:p.Ser472=
XM_017009485.1:c.1338C>T XP_016864974.1:p.Ser446=
XR_001742068.2:n.1858C>T
NM_005921.2:c.1827C>T MANE Select NP_005912.1:p.Ser609=