Canonical Allele Identifier: CA448954061
Gene: MYLIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.16145245T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16145014T>A , CM000668.2:g.16145014T>A GRCh38
NC_000006.11:g.16145245T>A , CM000668.1:g.16145245T>A GRCh37
NC_000006.10:g.16253224T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356840.8:c.945T>A MANE Select ENSP00000349298.3:p.Ile315=
ENST00000349606.4:c.402T>A ENSP00000008686.5:p.Ile134=
ENST00000356840.7:c.945T>A ENSP00000349298.3:p.Ile315=
NM_013262.3:c.945T>A NP_037394.2:p.Ile315=
XM_005249032.2:c.780T>A XP_005249089.1:p.Ile260=
XM_005249033.2:c.402T>A XP_005249090.1:p.Ile134=
XM_005249033.3:c.402T>A XP_005249090.1:p.Ile134=
XM_017010789.1:c.945T>A XP_016866278.1:p.Ile315=
NM_013262.4:c.945T>A MANE Select NP_037394.2:p.Ile315=
Search 100 bp 5'
Search 100 bp 3'