Canonical Allele Identifier: CA444399224
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1748218063
MyVariant Identifiers: chr5:g.56177640G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881813G>A , CM000667.2:g.56881813G>A GRCh38
NC_000005.9:g.56177640G>A , CM000667.1:g.56177640G>A GRCh37
NC_000005.8:g.56213397G>A NCBI36
NG_031884.1:g.71741G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2613G>A MANE Select ENSP00000382423.3:p.Leu871=
ENST00000399503.3:c.2613G>A ENSP00000382423.3:p.Leu871=
NM_005921.1:c.2613G>A NP_005912.1:p.Leu871=
XM_005248519.3:c.2235G>A XP_005248576.2:p.Leu745=
XM_011543406.1:c.2358G>A XP_011541708.1:p.Leu786=
XM_011543407.1:c.2334G>A XP_011541709.1:p.Leu778=
XM_011543408.1:c.2613G>A XP_011541710.1:p.Leu871=
XM_017009484.1:c.2202G>A XP_016864973.1:p.Leu734=
XM_017009485.1:c.2124G>A XP_016864974.1:p.Leu708=
XR_001742068.2:n.2644G>A
NM_005921.2:c.2613G>A MANE Select NP_005912.1:p.Leu871=