Canonical Allele Identifier: CA1621068919
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823755A= , CM000668.2:g.35823755A= GRCh38
NC_000006.11:g.35791532A= , CM000668.1:g.35791532A= GRCh37
NC_000006.10:g.35899510A= NCBI36
NG_012184.1:g.23462A=
NG_012184.2:g.23462A=
NG_012184.3:g.31550A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*790A= MANE Select ENSP00000353346.1:n.*790A=
ENST00000496656.2:n.578+3935A=
ENST00000651132.1:c.*790A= ENSP00000498322.1:n.*790A=
ENST00000651676.1:c.*16+4292A= ENSP00000498699.1:n.*16+4292A=
ENST00000651994.1:c.*870A= ENSP00000498310.1:n.*870A=
ENST00000652718.1:c.508+4292A= ENSP00000498866.1:n.508+4292A=
ENST00000360215.2:c.*790A= ENSP00000353346.1:n.*790A=
ENST00000496656.1:n.812+3935A=
NM_182548.3:c.*790A= NP_872354.1:n.*790A=
NM_182548.4:c.*790A= MANE Select NP_872354.1:n.*790A=