Canonical Allele Identifier: CA917723925

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1554147856

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823478_35823479insACACACTCTCTCTCTC , CM000668.2:g.35823478_35823479insACACACTCTCTCTCTC	GRCh38
NC_000006.11:g.35791255_35791256insACACACTCTCTCTCTC , CM000668.1:g.35791255_35791256insACACACTCTCTCTCTC	GRCh37
NC_000006.10:g.35899233_35899234insACACACTCTCTCTCTC	NCBI36
NG_012184.1:g.23185_23186insACACACTCTCTCTCTC
NG_012184.2:g.23185_23186insACACACTCTCTCTCTC
NG_012184.3:g.31273_31274insACACACTCTCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*513_*514insACACACTCTCTCTCTC MANE Select	ENSP00000353346.1:n.*513_*514insACACACTCTCTCTCTC
ENST00000496656.2:n.578+3658_578+3659insACACACTCTCTCTCTC
ENST00000651132.1:c.*513_*514insACACACTCTCTCTCTC	ENSP00000498322.1:n.*513_*514insACACACTCTCTCTCTC
ENST00000651676.1:c.*16+4015_*16+4016insACACACTCTCTCTCTC	ENSP00000498699.1:n.*16+4015_*16+4016insACACACTCTCTCTCTC
ENST00000651994.1:c.*593_*594insACACACTCTCTCTCTC	ENSP00000498310.1:n.*593_*594insACACACTCTCTCTCTC
ENST00000652718.1:c.508+4015_508+4016insACACACTCTCTCTCTC	ENSP00000498866.1:n.508+4015_508+4016insACACACTCTCTCTCTC
ENST00000360215.2:c.*513_*514insACACACTCTCTCTCTC	ENSP00000353346.1:n.*513_*514insACACACTCTCTCTCTC
ENST00000496656.1:n.812+3658_812+3659insACACACTCTCTCTCTC
NM_182548.3:c.*513_*514insACACACTCTCTCTCTC	NP_872354.1:n.*513_*514insACACACTCTCTCTCTC
NM_182548.4:c.*513_*514insACACACTCTCTCTCTC MANE Select	NP_872354.1:n.*513_*514insACACACTCTCTCTCTC