Canonical Allele Identifier: CA1621068962

Gene: LHFPL5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823858_35823860delinsATT , CM000668.2:g.35823858_35823860delinsATT	GRCh38
NC_000006.11:g.35791635_35791637delinsATT , CM000668.1:g.35791635_35791637delinsATT	GRCh37
NC_000006.10:g.35899613_35899615delinsATT	NCBI36
NG_012184.1:g.23565_23567delinsATT
NG_012184.2:g.23565_23567delinsATT
NG_012184.3:g.31653_31655delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*893_*895delinsATT MANE Select	ENSP00000353346.1:n.*893_*895delinsATT
ENST00000496656.2:n.578+4038_578+4040delinsATT
ENST00000651132.1:c.*893_*895delinsATT	ENSP00000498322.1:n.*893_*895delinsATT
ENST00000651676.1:c.*16+4395_*16+4397delinsATT	ENSP00000498699.1:n.*16+4395_*16+4397delinsATT
ENST00000651994.1:c.*973_*975delinsATT	ENSP00000498310.1:n.*973_*975delinsATT
ENST00000652718.1:c.508+4395_508+4397delinsATT	ENSP00000498866.1:n.508+4395_508+4397delinsATT
ENST00000360215.2:c.*893_*895delinsATT	ENSP00000353346.1:n.*893_*895delinsATT
ENST00000496656.1:n.812+4038_812+4040delinsATT
NM_182548.3:c.*893_*895delinsATT	NP_872354.1:n.*893_*895delinsATT
NM_182548.4:c.*893_*895delinsATT MANE Select	NP_872354.1:n.*893_*895delinsATT