Canonical Allele Identifier: CA450125617
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35773654G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805877G>C , CM000668.2:g.35805877G>C GRCh38
NC_000006.11:g.35773654G>C , CM000668.1:g.35773654G>C GRCh37
NC_000006.10:g.35881632G>C NCBI36
NG_012184.1:g.5584G>C
NG_012184.2:g.5584G>C
NG_012184.3:g.13672G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.207G>C MANE Select ENSP00000353346.1:p.Val69=
ENST00000651132.1:c.207G>C ENSP00000498322.1:p.Val69=
ENST00000651676.1:c.207G>C ENSP00000498699.1:p.Val69=
ENST00000651994.1:c.207G>C ENSP00000498310.1:p.Val69=
ENST00000652718.1:c.39G>C ENSP00000498866.1:p.Val13=
ENST00000360215.2:c.207G>C ENSP00000353346.1:p.Val69=
NM_182548.3:c.207G>C NP_872354.1:p.Val69=
XM_011514403.1:c.207G>C XP_011512705.1:p.Val69=
NM_182548.4:c.207G>C MANE Select NP_872354.1:p.Val69=
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