Canonical Allele Identifier: CA1621068867

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1768920668

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823635_35823636insC , CM000668.2:g.35823635_35823636insC	GRCh38
NC_000006.11:g.35791412_35791413insC , CM000668.1:g.35791412_35791413insC	GRCh37
NC_000006.10:g.35899390_35899391insC	NCBI36
NG_012184.1:g.23342_23343insC
NG_012184.2:g.23342_23343insC
NG_012184.3:g.31430_31431insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*670_*671insC MANE Select	ENSP00000353346.1:n.*670_*671insC
ENST00000496656.2:n.578+3815_578+3816insC
ENST00000651132.1:c.*670_*671insC	ENSP00000498322.1:n.*670_*671insC
ENST00000651676.1:c.*16+4172_*16+4173insC	ENSP00000498699.1:n.*16+4172_*16+4173insC
ENST00000651994.1:c.*750_*751insC	ENSP00000498310.1:n.*750_*751insC
ENST00000652718.1:c.508+4172_508+4173insC	ENSP00000498866.1:n.508+4172_508+4173insC
ENST00000360215.2:c.*670_*671insC	ENSP00000353346.1:n.*670_*671insC
ENST00000496656.1:n.812+3815_812+3816insC
NM_182548.3:c.*670_*671insC	NP_872354.1:n.*670_*671insC
NM_182548.4:c.*670_*671insC MANE Select	NP_872354.1:n.*670_*671insC