Canonical Allele Identifier: CA622937055

Gene: LCAT

Linked Data

• gnomAD v2: 16-67974736-TAC-T
• gnomAD v4: 16-67940833-TAC-T
• MyVariant Identifiers: chr16:g.67974737_67974738del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940835_67940836del , CM000678.2:g.67940835_67940836del	GRCh38
NC_000016.9:g.67974738_67974739del , CM000678.1:g.67974738_67974739del	GRCh37
NC_000016.8:g.66532239_66532240del	NCBI36
NG_009778.1:g.8278_8279del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-357_749-356del MANE Select	ENSP00000264005.5:n.749-357_749-356del
ENST00000264005.9:c.749-357_749-356del	ENSP00000264005.5:n.749-357_749-356del
ENST00000570369.5:c.156-761_156-760del
ENST00000570980.1:c.533-357_533-356del	ENSP00000464651.1:n.533-357_533-356del
ENST00000573538.5:c.392-4_392-3del	ENSP00000463220.1:n.392-4_392-3del
NM_000229.1:c.749-357_749-356del	NP_000220.1:n.749-357_749-356del
NM_000229.2:c.749-357_749-356del MANE Select	NP_000220.1:n.749-357_749-356del