Canonical Allele Identifier: CA364644027

Gene: LCA5

Linked Data

• dbSNP Id: rs866143416
• MyVariant Identifiers: chr6:g.80201386G>T (hg19) ; chr6:g.79491669G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79491669G>T , CM000668.2:g.79491669G>T	GRCh38
NC_000006.11:g.80201386G>T , CM000668.1:g.80201386G>T	GRCh37
NC_000006.10:g.80258105G>T	NCBI36
NG_016011.1:g.50762C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369846.9:c.1017C>A MANE Select	ENSP00000358861.4:p.Phe339Leu
ENST00000369846.8:c.1017C>A	ENSP00000358861.4:p.Phe339Leu
ENST00000392959.5:c.1017C>A	ENSP00000376686.1:p.Phe339Leu
ENST00000467898.3:c.1017C>A	ENSP00000474463.1:p.Phe339Leu
NM_001122769.2:c.1017C>A	NP_001116241.1:p.Phe339Leu
NM_181714.3:c.1017C>A	NP_859065.2:p.Phe339Leu
XM_005248665.3:c.1017C>A	XP_005248722.1:p.Phe339Leu
XM_011535504.1:c.1017C>A	XP_011533806.1:p.Phe339Leu
XM_005248665.4:c.1017C>A	XP_005248722.1:p.Phe339Leu
NM_001122769.3:c.1017C>A MANE Select	NP_001116241.1:p.Phe339Leu
NM_181714.4:c.1017C>A	NP_859065.2:p.Phe339Leu