Canonical Allele Identifier: CA2633851411

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940613-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940613_67940614insA , CM000678.2:g.67940613_67940614insA	GRCh38
NC_000016.9:g.67974516_67974517insA , CM000678.1:g.67974516_67974517insA	GRCh37
NC_000016.8:g.66532017_66532018insA	NCBI36
NG_009778.1:g.8499_8500insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-136_749-135insT MANE Select	ENSP00000264005.5:n.749-136_749-135insT
ENST00000264005.9:c.749-136_749-135insT	ENSP00000264005.5:n.749-136_749-135insT
ENST00000570369.5:c.156-540_156-539insT
ENST00000570980.1:c.533-136_533-135insT	ENSP00000464651.1:n.533-136_533-135insT
ENST00000573538.5:c.486+123_486+124insT	ENSP00000463220.1:n.486+123_486+124insT
NM_000229.1:c.749-136_749-135insT	NP_000220.1:n.749-136_749-135insT
NM_000229.2:c.749-136_749-135insT MANE Select	NP_000220.1:n.749-136_749-135insT