Canonical Allele Identifier: CA2633851750

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940754-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940754_67940755insG , CM000678.2:g.67940754_67940755insG	GRCh38
NC_000016.9:g.67974657_67974658insG , CM000678.1:g.67974657_67974658insG	GRCh37
NC_000016.8:g.66532158_66532159insG	NCBI36
NG_009778.1:g.8358_8359insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-277_749-276insC MANE Select	ENSP00000264005.5:n.749-277_749-276insC
ENST00000264005.9:c.749-277_749-276insC	ENSP00000264005.5:n.749-277_749-276insC
ENST00000570369.5:c.156-681_156-680insC
ENST00000570980.1:c.533-277_533-276insC	ENSP00000464651.1:n.533-277_533-276insC
ENST00000573538.5:c.468_469insC	ENSP00000463220.1:n.468_469insC
NM_000229.1:c.749-277_749-276insC	NP_000220.1:n.749-277_749-276insC
NM_000229.2:c.749-277_749-276insC MANE Select	NP_000220.1:n.749-277_749-276insC