Canonical Allele Identifier: CA1619211477

Gene: LTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31570550_31570551delinsCT , CM000668.2:g.31570550_31570551delinsCT	GRCh38
NC_000006.11:g.31538327_31538328delinsCT , CM000668.1:g.31538327_31538328delinsCT	GRCh37
NC_000006.10:g.31646306_31646307delinsCT	NCBI36
NG_012010.1:g.3452_3453delinsCT

Transcript Alleles

HGVS	Amino-acid change
XM_011514614.1:c.-341-942_-341-941delinsCT	XP_011512916.1:n.-341-942_-341-941delinsCT
XM_011514615.1:c.-341-942_-341-941delinsCT	XP_011512917.1:n.-341-942_-341-941delinsCT
XM_011514616.1:c.-177-1585_-177-1584delinsCT	XP_011512918.1:n.-177-1585_-177-1584delinsCT
XM_011514617.1:c.-341-942_-341-941delinsCT	XP_011512919.1:n.-341-942_-341-941delinsCT
XM_011514618.1:c.-341-942_-341-941delinsCT	XP_011512920.1:n.-341-942_-341-941delinsCT
XR_926695.1:n.116+2032_116+2033delinsAG
NR_149045.1:n.121+2032_121+2033delinsAG
XM_011514615.2:c.-341-942_-341-941delinsCT	XP_011512917.1:n.-341-942_-341-941delinsCT
XM_011514616.2:c.-177-1585_-177-1584delinsCT	XP_011512918.1:n.-177-1585_-177-1584delinsCT
XM_011514617.2:c.-341-942_-341-941delinsCT	XP_011512919.1:n.-341-942_-341-941delinsCT