Canonical Allele Identifier: CA824259913
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1271031207
MyVariant Identifiers: chr6:g.35791677T>C (hg19) chr6:g.35823900T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823900T>C , CM000668.2:g.35823900T>C GRCh38
NC_000006.11:g.35791677T>C , CM000668.1:g.35791677T>C GRCh37
NC_000006.10:g.35899655T>C NCBI36
NG_012184.1:g.23607T>C
NG_012184.2:g.23607T>C
NG_012184.3:g.31695T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*935T>C MANE Select ENSP00000353346.1:n.*935T>C
ENST00000496656.2:n.578+4080T>C
ENST00000651132.1:c.*935T>C ENSP00000498322.1:n.*935T>C
ENST00000651676.1:c.*16+4437T>C ENSP00000498699.1:n.*16+4437T>C
ENST00000652718.1:c.508+4437T>C ENSP00000498866.1:n.508+4437T>C
ENST00000360215.2:c.*935T>C ENSP00000353346.1:n.*935T>C
ENST00000496656.1:n.812+4080T>C
NM_182548.3:c.*935T>C NP_872354.1:n.*935T>C
NM_182548.4:c.*935T>C MANE Select NP_872354.1:n.*935T>C
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