Canonical Allele Identifier: CA359781340
Gene: MAP3K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.56171095G>C (hg19) chr5:g.56875268G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875268G>C , CM000667.2:g.56875268G>C GRCh38
NC_000005.9:g.56171095G>C , CM000667.1:g.56171095G>C GRCh37
NC_000005.8:g.56206852G>C NCBI36
NG_031884.1:g.65196G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1923G>C MANE Select ENSP00000382423.3:p.Met641Ile
ENST00000399503.3:c.1923G>C ENSP00000382423.3:p.Met641Ile
NM_005921.1:c.1923G>C NP_005912.1:p.Met641Ile
XM_005248519.3:c.1545G>C XP_005248576.2:p.Met515Ile
XM_011543406.1:c.1668G>C XP_011541708.1:p.Met556Ile
XM_011543407.1:c.1686+2263G>C XP_011541709.1:n.1686+2263G>C
XM_011543408.1:c.1923G>C XP_011541710.1:p.Met641Ile
XM_017009484.1:c.1512G>C XP_016864973.1:p.Met504Ile
XM_017009485.1:c.1434G>C XP_016864974.1:p.Met478Ile
XR_001742068.2:n.1954G>C
NM_005921.2:c.1923G>C MANE Select NP_005912.1:p.Met641Ile
Search 100 bp 5'
Search 100 bp 3'