Canonical Allele Identifier: CA450125309
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35782552T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814775T>C , CM000668.2:g.35814775T>C GRCh38
NC_000006.11:g.35782552T>C , CM000668.1:g.35782552T>C GRCh37
NC_000006.10:g.35890530T>C NCBI36
NG_012184.1:g.14482T>C
NG_012184.2:g.14482T>C
NG_012184.3:g.22570T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.642T>C MANE Select ENSP00000353346.1:p.Asp214=
ENST00000496656.2:n.421T>C
ENST00000651132.1:c.642T>C ENSP00000498322.1:p.Asp214=
ENST00000651676.1:c.642T>C ENSP00000498699.1:p.Asp214=
ENST00000651994.1:c.*70-4662T>C ENSP00000498310.1:n.*70-4662T>C
ENST00000652718.1:c.474T>C ENSP00000498866.1:p.Asp158=
ENST00000360215.2:c.642T>C ENSP00000353346.1:p.Asp214=
ENST00000496656.1:n.421T>C
NM_182548.3:c.642T>C NP_872354.1:p.Asp214=
XM_011514403.1:c.642T>C XP_011512705.1:p.Asp214=
NM_182548.4:c.642T>C MANE Select NP_872354.1:p.Asp214=