Canonical Allele Identifier: CA450125108

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1768725153
• MyVariant Identifiers: chr6:g.35782357T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814580T>C , CM000668.2:g.35814580T>C	GRCh38
NC_000006.11:g.35782357T>C , CM000668.1:g.35782357T>C	GRCh37
NC_000006.10:g.35890335T>C	NCBI36
NG_012184.1:g.14287T>C
NG_012184.2:g.14287T>C
NG_012184.3:g.22375T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.447T>C MANE Select	ENSP00000353346.1:p.Pro149=
ENST00000496656.2:n.226T>C
ENST00000651132.1:c.447T>C	ENSP00000498322.1:p.Pro149=
ENST00000651676.1:c.447T>C	ENSP00000498699.1:p.Pro149=
ENST00000651994.1:c.*70-4857T>C	ENSP00000498310.1:n.*70-4857T>C
ENST00000652718.1:c.279T>C	ENSP00000498866.1:p.Pro93=
ENST00000360215.2:c.447T>C	ENSP00000353346.1:p.Pro149=
ENST00000496656.1:n.226T>C
NM_182548.3:c.447T>C	NP_872354.1:p.Pro149=
XM_011514403.1:c.447T>C	XP_011512705.1:p.Pro149=
NM_182548.4:c.447T>C MANE Select	NP_872354.1:p.Pro149=