Canonical Allele Identifier: CA1621068961

Gene: LHFPL5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823857_35823858delinsCA , CM000668.2:g.35823857_35823858delinsCA	GRCh38
NC_000006.11:g.35791634_35791635delinsCA , CM000668.1:g.35791634_35791635delinsCA	GRCh37
NC_000006.10:g.35899612_35899613delinsCA	NCBI36
NG_012184.1:g.23564_23565delinsCA
NG_012184.2:g.23564_23565delinsCA
NG_012184.3:g.31652_31653delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*892_*893delinsCA MANE Select	ENSP00000353346.1:n.*892_*893delinsCA
ENST00000496656.2:n.578+4037_578+4038delinsCA
ENST00000651132.1:c.*892_*893delinsCA	ENSP00000498322.1:n.*892_*893delinsCA
ENST00000651676.1:c.*16+4394_*16+4395delinsCA	ENSP00000498699.1:n.*16+4394_*16+4395delinsCA
ENST00000651994.1:c.*972_*973delinsCA	ENSP00000498310.1:n.*972_*973delinsCA
ENST00000652718.1:c.508+4394_508+4395delinsCA	ENSP00000498866.1:n.508+4394_508+4395delinsCA
ENST00000360215.2:c.*892_*893delinsCA	ENSP00000353346.1:n.*892_*893delinsCA
ENST00000496656.1:n.812+4037_812+4038delinsCA
NM_182548.3:c.*892_*893delinsCA	NP_872354.1:n.*892_*893delinsCA
NM_182548.4:c.*892_*893delinsCA MANE Select	NP_872354.1:n.*892_*893delinsCA