Canonical Allele Identifier: CA363784770

Gene: LHFPL5

Linked Data

• MyVariant Identifiers: chr6:g.35773746T>C (hg19) ; chr6:g.35805969T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35805969T>C , CM000668.2:g.35805969T>C	GRCh38
NC_000006.11:g.35773746T>C , CM000668.1:g.35773746T>C	GRCh37
NC_000006.10:g.35881724T>C	NCBI36
NG_012184.1:g.5676T>C
NG_012184.2:g.5676T>C
NG_012184.3:g.13764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.299T>C MANE Select	ENSP00000353346.1:p.Phe100Ser
ENST00000651132.1:c.299T>C	ENSP00000498322.1:p.Phe100Ser
ENST00000651676.1:c.299T>C	ENSP00000498699.1:p.Phe100Ser
ENST00000651994.1:c.299T>C	ENSP00000498310.1:p.Phe100Ser
ENST00000652718.1:c.131T>C	ENSP00000498866.1:p.Phe44Ser
ENST00000360215.2:c.299T>C	ENSP00000353346.1:p.Phe100Ser
NM_182548.3:c.299T>C	NP_872354.1:p.Phe100Ser
XM_011514403.1:c.299T>C	XP_011512705.1:p.Phe100Ser
NM_182548.4:c.299T>C MANE Select	NP_872354.1:p.Phe100Ser