Canonical Allele Identifier: CA283163055

Gene: LCAT

Linked Data

• dbSNP Id: rs17287348
• MyVariant Identifiers: chr16:g.67976698T>G (hg19) ; chr16:g.67942795T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942795T>G , CM000678.2:g.67942795T>G	GRCh38
NC_000016.9:g.67976698T>G , CM000678.1:g.67976698T>G	GRCh37
NC_000016.8:g.66534199T>G	NCBI36
NG_009778.1:g.6318A>C
NG_033098.1:g.30900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.428-29A>C MANE Select	ENSP00000264005.5:n.428-29A>C
ENST00000264005.9:c.428-29A>C	ENSP00000264005.5:n.428-29A>C
ENST00000570369.5:c.155+66A>C
ENST00000570980.1:c.212-29A>C	ENSP00000464651.1:n.212-29A>C
ENST00000573538.5:c.71-29A>C	ENSP00000463220.1:n.71-29A>C
ENST00000573846.1:n.42-29A>C
ENST00000575277.1:n.206-29A>C
ENST00000575467.5:c.*123-29A>C	ENSP00000460653.1:n.*123-29A>C
NM_000229.1:c.428-29A>C	NP_000220.1:n.428-29A>C
NM_000229.2:c.428-29A>C MANE Select	NP_000220.1:n.428-29A>C