Canonical Allele Identifier: CA1619208707

Gene: LTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31563495_31563497delinsACT , CM000668.2:g.31563495_31563497delinsACT	GRCh38
NC_000006.11:g.31531272_31531274delinsACT , CM000668.1:g.31531272_31531274delinsACT	GRCh37
NC_000006.10:g.31639251_31639253delinsACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011514614.1:c.-342+2226_-342+2228delinsACT	XP_011512916.1:n.-342+2226_-342+2228delinsACT
XM_011514615.1:c.-342+1028_-342+1030delinsACT	XP_011512917.1:n.-342+1028_-342+1030delinsACT
XM_011514616.1:c.-178+2226_-178+2228delinsACT	XP_011512918.1:n.-178+2226_-178+2228delinsACT
XM_011514617.1:c.-342+2226_-342+2228delinsACT	XP_011512919.1:n.-342+2226_-342+2228delinsACT
XM_011514618.1:c.-342+2226_-342+2228delinsACT	XP_011512920.1:n.-342+2226_-342+2228delinsACT
XR_926695.1:n.116+9086_116+9088delinsAGT
NR_149045.1:n.122-2775_122-2773delinsAGT
XM_011514615.2:c.-342+1028_-342+1030delinsACT	XP_011512917.1:n.-342+1028_-342+1030delinsACT
XM_011514616.2:c.-178+2226_-178+2228delinsACT	XP_011512918.1:n.-178+2226_-178+2228delinsACT
XM_011514617.2:c.-342+2226_-342+2228delinsACT	XP_011512919.1:n.-342+2226_-342+2228delinsACT