Canonical Allele Identifier: CA396376043

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940298-T-A
• MyVariant Identifiers: chr16:g.67974201T>A (hg19) ; chr16:g.67940298T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940298T>A , CM000678.2:g.67940298T>A	GRCh38
NC_000016.9:g.67974201T>A , CM000678.1:g.67974201T>A	GRCh37
NC_000016.8:g.66531702T>A	NCBI36
NG_009778.1:g.8815A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.929A>T MANE Select	ENSP00000264005.5:p.His310Leu
ENST00000264005.9:c.929A>T	ENSP00000264005.5:p.His310Leu
ENST00000570369.5:c.156-224A>T
ENST00000570980.1:c.713A>T	ENSP00000464651.1:p.His238Leu
ENST00000573538.5:c.667A>T	ENSP00000463220.1:n.667A>T
NM_000229.1:c.929A>T	NP_000220.1:p.His310Leu
NM_000229.2:c.929A>T MANE Select	NP_000220.1:p.His310Leu